Medical device recalls

5261 recalls on record · updated June 11, 2026

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Dexcom, Inc. recalls Dexcom G7 — Continuous Glucose Monitoring System

May 29, 2026 · Medical device recalls Sensors identified as scrap were diverted and sold by third-party — Defect

Insulet Corporation, Inc. recalls Omnipod — Device intended for the subcutaneous delivery of insulin into a patient

May 26, 2026 · Medical device recalls Manufacturing issue that could result in under delivery of insulin — Defect

Medtronic Neuromodulation recalls Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkin…

May 13, 2026 · Medical device recalls Moderate risk A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled wit…

Medtronic Neuromodulation recalls Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkin…

May 13, 2026 · Medical device recalls Moderate risk A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled wit…

Trividia Health, Inc. recalls TRUE METRIX — Blood Glucose Monitoring Systems

May 5, 2026 · Medical device recalls As currently written, the Owner’s Booklets/System Instructions for Use fails to…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR…

April 30, 2026 · Medical device recalls Moderate risk It was identified that HDDs used in the PCs of Azurion and Allura systems may s…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222)…

April 30, 2026 · Medical device recalls Moderate risk It was identified that HDDs used in the PCs of Azurion and Allura systems may s…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Allura system; System Code Description (Model Numbers): Allura Xper FD10C (722001), Allura Xper FD10F (722002), Allura…

April 28, 2026 · Medical device recalls Moderate risk The deaeration hose in X-ray tube cooling units type CU3101, manufactured betwe…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Inte…

April 28, 2026 · Medical device recalls Moderate risk The deaeration hose in X-ray tube cooling units type CU3101, manufactured betwe…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions a…

April 28, 2026 · Medical device recalls Moderate risk Potential safety issue with Philips Azurion systems, where longitudinal and tra…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12…

April 28, 2026 · Medical device recalls Moderate risk The deaeration hose in X-ray tube cooling units type CU3101, manufactured betwe…

GE Medical Systems Information Technologies Inc recalls GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with Ape…

April 24, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of an unlikely situation where potential loss of…

GE Medical Systems Information Technologies Inc recalls GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-…

April 24, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of an unlikely situation where potential loss of…

GE Medical Systems Information Technologies Inc recalls GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Teleme…

April 24, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of an unlikely situation where potential loss of…

Devicor Medical Products Inc recalls HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3

April 24, 2026 · Medical device recalls Moderate risk Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may conta…

GE Medical Systems Information Technologies Inc recalls GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction…

April 24, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of an unlikely situation where potential loss of…

GE Medical Systems Information Technologies Inc recalls GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCA…

April 24, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of an unlikely situation where potential loss of…

GE Medical Systems Information Technologies Inc recalls GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used i…

April 24, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of an unlikely situation where potential loss of…

C.R. Bard Inc recalls Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley Cat…

April 23, 2026 · Medical device recalls Moderate risk Due to stain present on the surface of affected foley catheters.

Novapproach Spine, LLC recalls OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Small 7 Degree 10mm X 7…

April 23, 2026 · Medical device recalls Moderate risk Intervertebral body fusion system straight inserter failed to properly attach t…

Bolton Medical Inc. recalls RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U 28-N4-32-164-…

April 22, 2026 · Medical device recalls High risk Labeling update concerning proximal clasp disconnection from the outer control…

BioFire Joint Infection Panel REF: RFIT-ASY-0138 recalled over fire hazard

April 22, 2026 · Medical device recalls Moderate risk Contamination to in-vitro diagnostic test may result in false positives.

Medtronic Perfusion Systems recalls Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmonary bypass vascular ca…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular cathe…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Cardiopulmonary bypass vascular cathet…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular cathet…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular cathet…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular ca…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass vascular cathe…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular cathet…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Medtronic Perfusion Systems recalls Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular cathet…

April 21, 2026 · Medical device recalls Moderate risk Certain lots of product have the potential for a sterile barrier breach.

Windstone Medical Packaging dba Aligned Medical Solutions recalls Aligned Medical Angio Pack — Angio Packs (AMS6908E and AMS6908F)

April 20, 2026 · Medical device recalls Risk of the syringe rotating adapter unwinding during use, which may result in…

Abiomed, Inc. recalls Automated Impella Controller (AIC); Product Code: 0042-0000-US;

April 20, 2026 · Medical device recalls High risk A retrospective review identified that there are AIC units requiring specific h…

Dexcom, Inc. recalls Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ iOS CGM App Model/Catalog Number…

April 14, 2026 · Medical device recalls Moderate risk A software defect in which a low-priority file I/O check blocks the higher-prio…

Dexcom, Inc. recalls Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number: SW…

April 14, 2026 · Medical device recalls Moderate risk A software defect in which a low-priority file I/O check blocks the higher-prio…

Dexcom, Inc. recalls Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog Number…

April 14, 2026 · Medical device recalls Moderate risk A software defect in which a low-priority file I/O check blocks the higher-prio…

Philips North America recalls Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781260. 2. Model Number (REF):…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781270. 2. Model Number…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. Model Number (REF): 782109. 3.…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF): 781357. 2. Model Number (REF): 782106. 3.…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (REF): 782116 2. Model Number (REF): 782148.…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781278.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120. 2. Model Number (REF): 782153.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781315. 2. Model Number (REF): 781341. 3. Model…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Number (REF): 781178.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 781271. 2. Model Number (REF): 782105. 510(k…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 781358. 2. Model Number (REF): 782107. 3.…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 781262.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 781196. 2. Model Number (REF): 781296.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia Ambition S with MR Elastography (MRE). 1. Model Number (REF): 781359. 2. Model Number (REF): 782108. 3.…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Evolution upgrade 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782143. 2. Model Number (REF): 782162.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 781342. 2. Model Number (REF): 781377. 3. Model…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 782118. 2. Model Number (REF)…

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

Philips North America recalls Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.

April 14, 2026 · Medical device recalls Moderate risk The potential for stiffness value errors when a specific range of image reconst…

O&M HALYARD INC recalls Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.),…

April 13, 2026 · Medical device recalls Moderate risk Nitrile Exam Glove failed to meet specifications chemical permeation performanc…

Jolife AB recalls LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Nu…

April 13, 2026 · Medical device recalls Moderate risk Due to a subset of chest compression systems/devices where the service performe…

Physio-Control, Inc. recalls LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 9957…

April 13, 2026 · Medical device recalls Moderate risk Some defibrillators serviced between July 2023 through November 2025 were servi…

Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) PAIN TRAY, Medline Kit SKU…

April 10, 2026 · Medical device recalls High risk Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dex…

Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) ANESTHESIA TRAY, Medline S…

April 10, 2026 · Medical device recalls High risk Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dex…

Medline Industries, LP recalls Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P

April 10, 2026 · Medical device recalls Moderate risk Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes,…

Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL TRAY W/PENCIL POINT…

April 10, 2026 · Medical device recalls High risk Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dex…

Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF,…

April 10, 2026 · Medical device recalls High risk Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dex…

Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S B…

April 10, 2026 · Medical device recalls High risk Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dex…

Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL BLOCK TRAY, Medline…

April 10, 2026 · Medical device recalls High risk Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dex…

Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit SK…

April 10, 2026 · Medical device recalls High risk Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dex…

Stryker Sustainability Solutions recalls BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls BARD Dynamic XT Steerable, Product Number 201103, REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401652; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Integra LifeSciences Corp. (NeuroSciences) recalls Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD Cath…

April 10, 2026 · Medical device recalls Moderate risk Out-of-specification endotoxin result that did not meet the acceptance criteria.

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401582; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

ARROW INTERNATIONAL, LLC recalls Cannon II Plus Hemodialysis Catheter, REF: CS-15242-VSP, CS-15282-VSP, CS-15322-VSP, CS-15362-VSP, CS-15552-VSP, CSD-15…

April 10, 2026 · Medical device recalls High risk 16F dual-valved splittable sheath introducer, the subject of a supplier recall,…

Stryker Sustainability Solutions recalls Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401905; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

ARROW INTERNATIONAL, LLC recalls NextStep Antegrade Chronic Hemodialysis Catheter, REF: AC-15192-SFX, AC-15232-SFX, CS-15192-SFX, CS-15232-SFX, CS-15272…

April 10, 2026 · Medical device recalls High risk 16F dual-valved splittable sheath introducer, the subject of a supplier recall,…

ARROW INTERNATIONAL, LLC recalls Arrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS-15322-I

April 10, 2026 · Medical device recalls High risk 16F dual-valved splittable sheath introducer, the subject of a supplier recall,…

ARROW INTERNATIONAL, LLC recalls Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI, ACS-15232-VFI, ACS-15272-VFI, CS-15…

April 10, 2026 · Medical device recalls High risk 16F dual-valved splittable sheath introducer, the subject of a supplier recall,…

Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable, Product Number 200344; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Sustainability Solutions recalls BARD Dynamic Tip Steerable, Product Number 6DYNTP001;

April 10, 2026 · Medical device recalls Moderate risk Incomplete seals on sterile product

Stryker Corporation recalls Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be…

April 9, 2026 · Medical device recalls Moderate risk Due to nonconforming products being inadvertently distributed.

Becton, Dickinson and Company recalls Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7, 8…

April 8, 2026 · Medical device recalls Moderate risk Catheters may, due to a manufacturing process and material changes, leak/break…

Becton, Dickinson and Company recalls Swan-Ganz Pacing Catheter, Models: D200F7;

April 8, 2026 · Medical device recalls Moderate risk Catheters may, due to a manufacturing process and material changes, leak/break…

Becton, Dickinson and Company recalls Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P

April 8, 2026 · Medical device recalls Moderate risk Catheters may, due to a manufacturing process and material changes, leak/break…

Hologic, Inc recalls 3DIMENSIONS MAMMOGRAPHY SYSTEM; Model Numbers: 3DM-SYS-INTL2D, 3DM-SYS-INTL2D-MOB, 3DM-SYS-INTL2D-NS, 3DM-SYS-INTL3D, 3…

April 8, 2026 · Medical device recalls Moderate risk Complaints have been received of systems developing loose, missing, or broken i…

Medtronic Neuromodulation recalls Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devic…

April 8, 2026 · Medical device recalls Moderate risk Software issue: When programming the SynchroMed Pump with the A810 CP App in Fl…

Hologic, Inc recalls SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-SYS-3000-3D, SDM-SYS-6000-2D, SDM-SYS-6…

April 8, 2026 · Medical device recalls Moderate risk Complaints have been received of systems developing loose, missing, or broken i…

Becton Dickinson & Co. recalls BD GasPak EZ Campy Pouch System. Catalog Number: 260685. for microbiologic use

April 7, 2026 · Medical device recalls Moderate risk BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak…

Becton Dickinson & Co. recalls BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use

April 7, 2026 · Medical device recalls Moderate risk BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak…

Quidel Corporation recalls QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.

April 6, 2026 · Medical device recalls Moderate risk Product has the potential for false positive results

MICROVENTION INC. recalls LVIS Intraluminal Support Device, REF/Outside Diameter(OD)xTotal Length(TL)xWorking Length(WL): 214022-CAS/4.0 mm x 22…

April 6, 2026 · Medical device recalls Moderate risk Stent-assisted coiling device may due to commingling during manufacturing have…

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 4 CEM. Part Number: 150450204.

April 3, 2026 · Medical device recalls Moderate risk The external sterile packaging was found adhered to the internal sterile packag…

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.

April 3, 2026 · Medical device recalls Moderate risk The external sterile packaging was found adhered to the internal sterile packag…

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 7 CEM. Part Number: 150450207.

April 3, 2026 · Medical device recalls Moderate risk The external sterile packaging was found adhered to the internal sterile packag…

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 3 CEM. Part Number: 150450203.

April 3, 2026 · Medical device recalls Moderate risk The external sterile packaging was found adhered to the internal sterile packag…

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 7 CEM. Part Number: 150450107.

April 3, 2026 · Medical device recalls Moderate risk The external sterile packaging was found adhered to the internal sterile packag…

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 8 CEM. Part Number: 150450208.

April 3, 2026 · Medical device recalls Moderate risk The external sterile packaging was found adhered to the internal sterile packag…

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL RT SZ 5 CEM. Part Number: 150450205.

April 3, 2026 · Medical device recalls Moderate risk The external sterile packaging was found adhered to the internal sterile packag…

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 5 CEM. Part Number: 150450105.

April 3, 2026 · Medical device recalls Moderate risk The external sterile packaging was found adhered to the internal sterile packag…

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.

April 3, 2026 · Medical device recalls Moderate risk The external sterile packaging was found adhered to the internal sterile packag…

Windstone Medical Packaging, Inc. recalls Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes with Rotating Adapter (Namic RA…

April 2, 2026 · Medical device recalls High risk Affected kits contain Medline Namic RA Syringes, which are recalled by their ma…

Cook Incorporated recalls Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G31213 NR5.0-35-100-P-10S-0-CSC-20 G31214 NR5.…

April 2, 2026 · Medical device recalls High risk Marker bands may be at an increased risk of cracking/breakage. Potential advers…

Cook Incorporated recalls Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 Sizing catheters are single-use, steri…

April 2, 2026 · Medical device recalls High risk Marker bands may be at an increased risk of cracking/breakage. Potential advers…

Cook Incorporated recalls Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures are…

April 2, 2026 · Medical device recalls High risk Marker bands may be at an increased risk of cracking/breakage. Potential advers…

DFI Co., Ltd. recalls One Step UTI in vitro diagnostic test REF: 3374

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls One Step 10A in vitro diagnostic test

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

Intuitive Surgical, Inc. recalls Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X, Xi Surgical System Model/Catalog Number: IS4000; IS420…

April 2, 2026 · Medical device recalls Moderate risk Due to manipulator containing screws with in the arm sub-assembly that my be su…

DFI Co., Ltd. recalls One Step pH in vitro diagnostic test REF: 31I4P

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls One Step P in vitro diagnostic test REF: 8194

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls QUCARE Total Cholesterol in vitro diagnostic test REF: 6407

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls Uric Acid in vitro diagnostic test REF: 31H0P

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

DFI Co., Ltd. recalls One Step K in vitro diagnostic test REF: 81A4

April 2, 2026 · Medical device recalls Moderate risk The devices were distributed without required FDA premarket clearance or approv…

Merit Medical Systems, Inc. recalls Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY

April 2, 2026 · Medical device recalls Moderate risk catheter may experience resistance when being advanced over the guidewire

Merit Medical Systems, Inc. recalls Philips Bridge Prep Kit REF: K12-09098B Sterile EO, Rx ONLY

April 2, 2026 · Medical device recalls Moderate risk catheter may experience resistance when being advanced over the guidewire

Siemens Healthcare Diagnostics Inc recalls epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515;

April 2, 2026 · Medical device recalls Moderate risk Use of the affected product can result in discrepant low pH and measured Total…

Merit Medical Systems, Inc. recalls Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY

April 2, 2026 · Medical device recalls Moderate risk catheter may experience resistance when being advanced over the guidewire

Aniara Diagnostica LLC recalls ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A

April 1, 2026 · Medical device recalls Moderate risk Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market…

Biofire Spotfire Respiratory/Sore Throat Panel REF recalled over fire hazard

April 1, 2026 · Medical device recalls Moderate risk Respiratory/sore throat panel test may result in false negative results and con…

Abbott Point Of Care Inc. recalls i-STAT EG6+ cartridge; List Number: 03P77-25;

April 1, 2026 · Medical device recalls Moderate risk Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-2…

Abbott Point Of Care Inc. recalls i-STAT EG7+ cartridge; List Number: 03P76-25;

April 1, 2026 · Medical device recalls Moderate risk Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-2…

Abbott Point Of Care Inc. recalls i-STAT G3+ cartridge; List Number: 03P78-26;

April 1, 2026 · Medical device recalls Moderate risk Approximately 7.6% of cartridges from specific i-STAT EG7+ (list number 03P76-2…

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222, 722230)…

March 31, 2026 · Medical device recalls Moderate risk Potential for the bolts and plastic parts of the Cable Hose Carriers that hold…

Erbe Medical, LLC recalls ERBEFLO 2, Endoscopy Pump Tubing/Cap Set, REF: 20325-222

March 31, 2026 · Medical device recalls Moderate risk Devices providing sterile water/CO2/air to endoscopes were manufactured with a…

Erbe Medical, LLC recalls ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes, 20325-201; ERBEFLO CleverCap Hybrid Tubing/Cap Set for Fuj…

March 31, 2026 · Medical device recalls Moderate risk Devices providing sterile water/CO2/air to endoscopes were manufactured with a…

Erbe Medical, LLC recalls ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2 Tubing/Ca…

March 31, 2026 · Medical device recalls Moderate risk Devices providing sterile water/CO2/air to endoscopes were manufactured with a…

Boston Scientific Corporation recalls LUX-Dx II Plus, Arrythmia detector and alarm, Model M312, with SERVER SW LATITUDE DRAGON EU (Europe), Model 6446, Versi…

March 30, 2026 · Medical device recalls Moderate risk For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M31…

Boston Scientific Corporation recalls LUX-DX II, Arrythmia detector and alarm, Model M302, with SERVER SW LATITUDE DRAGON US, Model 6460, Version 7.5

March 30, 2026 · Medical device recalls Moderate risk For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M31…

Zimmer, Inc. recalls Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number: 00-5049-01…

March 30, 2026 · Medical device recalls Moderate risk Ten complaints have been received identifying issues at the time of use related…

Edwards Lifesciences, LLC recalls Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO

March 27, 2026 · Medical device recalls Moderate risk Labeling update to provide warning if functionality of the valve replacement de…

North American Rescue LLC. recalls AIDBAGs are first aid kits of convenience composed of individually labeled devices designed as specialty first aid kits…

March 27, 2026 · Medical device recalls High risk Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose…

Straumann USA LLC recalls Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous Dental Implant Abutments

March 27, 2026 · Medical device recalls Moderate risk Includes an incorrect screw seat interface.

Straumann USA LLC recalls Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158. Endosseous Dental Implant Abutments

March 27, 2026 · Medical device recalls Moderate risk Includes an incorrect screw seat interface.

Micro-X Ltd. recalls Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71

March 27, 2026 · Medical device recalls Moderate risk X-Ray generator may malfunction resulting in the X-Ray being inoperable.

GE Medical Systems, LLC recalls Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6

March 26, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of a potential security vulnerability impacting…

GE Medical Systems, LLC recalls Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25

March 26, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of a potential security vulnerability impacting…

GE Medical Systems, LLC recalls Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20

March 26, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of a potential security vulnerability impacting…

GE Medical Systems, LLC recalls Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23

March 26, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of a potential security vulnerability impacting…

GE Medical Systems, LLC recalls Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27

March 26, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of a potential security vulnerability impacting…

GE Medical Systems, LLC recalls Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-300

March 26, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of a potential security vulnerability impacting…

GE Medical Systems, LLC recalls Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15

March 26, 2026 · Medical device recalls Moderate risk GE HealthCare has become aware of a potential security vulnerability impacting…

Spacelabs Healthcare, Inc. recalls Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module Model/Catalog Number: 91496 Software…

March 26, 2026 · Medical device recalls Moderate risk Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester).

Immuno-Mycologics, Inc recalls Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens…

March 26, 2026 · Medical device recalls Moderate risk Neutralization Buffer may contain contaminants

Rolls of label stock used with the Omnicell i recalled over labeling errors

March 25, 2026 · Medical device recalls High risk Potential for mislabeled syringe produced by the i.v.STATION device.

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-27

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Number: DVF4016-25-S

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalog Number: DVF4019-25-S

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalog Number: DVF4022-25-S

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number: DVF4034-25

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-25-S

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog Number: DVF4034-27

March 25, 2026 · Medical device recalls Moderate risk Ophthalmic Tissue Forceps (DEX") are sterile, hand-held ophthalmic surgical ins…

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Orthorebirth Co Ltd recalls BioCera Fibers, Bioresorbable Bone Void Filler, REF: ORB-0320C-KC, ORB-0310C-KC, ORB-0304C-KC, ORB-0302C-KC, ORB-0305D-…

March 25, 2026 · Medical device recalls Moderate risk Resorbable bone void filler falls outside standard specifications.

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-25

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Orthorebirth Co Ltd recalls ZENBONE, REF: ORB-0320C-Z, ORB-0310C-Z, ORB-0304C-Z

March 25, 2026 · Medical device recalls Moderate risk Resorbable bone void filler falls outside standard specifications.

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/Catalog Number: DVF4014-25-S

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

VOCSN V+Pro package recalled over fire hazard

March 25, 2026 · Medical device recalls High risk Respiratory system intended to provide continuous/intermittent ventilator suppo…

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Number: DVF4019-23

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Katalyst Surgical, LLC recalls DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog Number: DVF4005-25

March 25, 2026 · Medical device recalls Moderate risk Field Safety Corrective Action for IFU in DEX Forceps and Scissors.

Heraeus Medical GmbH (Dental Division) recalls Heraeus, PALAMIX duo. Material Number: 66057897.

March 25, 2026 · Medical device recalls Based on long-term stability testing, it was determined that in units older tha…

Heraeus Medical GmbH (Dental Division) recalls Heraeus, PALAMIX uno. Material Number: 66057893.

March 25, 2026 · Medical device recalls Based on long-term stability testing, it was determined that in units older tha…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Oxoid Agglutinating Sera recalled over Salmonella risk

March 25, 2026 · Medical device recalls Moderate risk Affected lots are not performing to IFU criteria showing cross reactions with 2…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be included with the Olympus OER-…

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6 recalled over foreign material

March 25, 2026 · Medical device recalls Moderate risk Potential for product to contain foreign matter, confirmed to be inspect fragme…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2114.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113.

March 25, 2026 · Medical device recalls Moderate risk Potential for the Version 2 reprocessor connecting tube lock levers may fail pr…

Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115.

March 25, 2026 · Medical device recalls Moderate risk XXX

ICU Medical, Inc. recalls Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; ChemoLoc…

March 24, 2026 · Medical device recalls Moderate risk Oncology sets/closed system transfer devices with extension sets may leak resul…

Medline Industries, LP recalls Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. MTS,RT,HANDED/LFT,HRT,KIT, Medline Kit Numb…

March 24, 2026 · Medical device recalls High risk Medline has identified the presence of particulate within the fluid path of the…

Medline Industries, LP recalls Namic Preceptor Manifold, custom, Medline Product Number/SKU 64039307; Extravascular blood pressure transducer

March 24, 2026 · Medical device recalls High risk Medline has identified the presence of particulate within the fluid path of the…

Medline Industries, LP recalls Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038402; Cardiopulmonary bypass adaptor, stopcock, man…

March 24, 2026 · Medical device recalls High risk Medline has identified the presence of particulate within the fluid path of the…

Medline Industries, LP recalls Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, man…

March 24, 2026 · Medical device recalls High risk Medline has identified the presence of particulate within the fluid path of the…

Medline Industries, LP recalls Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038301; Cardiopulmonary bypass adaptor, stopcock, man…

March 24, 2026 · Medical device recalls High risk Medline has identified the presence of particulate within the fluid path of the…

Medline Industries, LP recalls 1. DBD-MTS,3V,MAN,KIT, Medline Kit Number/SKU 60010195; 2. MTS-LEFT HEART,KIT, Medline Kit Number/SKU 60033123; 3. MTS,…

March 24, 2026 · Medical device recalls High risk Medline has identified the presence of particulate within the fluid path of the…

Medline Industries, LP recalls 1. 3 VALVE MAN KIT, Medline Kit SKU Number: 65101544; 2. 3V MANIFOLD KIT, Medline Kit SKU Number: 65110351; 3. HEART CA…

March 24, 2026 · Medical device recalls High risk Medline has identified the presence of particulate within the fluid path of the…

Medline Industries, LP recalls Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SK…

March 24, 2026 · Medical device recalls High risk Medline has identified the presence of particulate within the fluid path of the…