Stryker Instruments Div. of Stryker Corporation recalls

84 recalls on record · latest: June 15, 2022

Official U.S. recall history for Stryker Instruments Div. of Stryker Corporation, compiled from official government records.

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Stryker Instruments Div. of Stryker Corporation recalls SurgiCount+ System Application, Software Version 2.0.17, Catalog Number 0694-002-090. Used for counting, displaying, re…

June 15, 2022 · Medical device recalls Moderate risk When scanning sponges out after a surgical procedure, an error may allow for a…

Stryker Zyphr Disposable Cranial Perforator recalled over possible metal fragments

October 16, 2020 · Medical device recalls Moderate risk Potential for the inner bit to contain a crack, that may or may not be visible,…

Stryker Instruments Div. of Stryker Corporation recalls Neptune E-SEP 165mm Blade Electrode, Catalog Number 0703-165-001 - Product Usage: The Neptune E-SEP is an Integrated Sm…

March 26, 2020 · Medical device recalls Moderate risk Due to a distribution error, product from the affected lot was shipped expired.

Stryker Instruments Div. of Stryker Corporation recalls Triton Canister System (finished part numbers FG 12009, for 3L canisters, and FG 12019 for 2L canisters) Scanning Label…

January 22, 2020 · Medical device recalls Moderate risk Some Canister Scanning Labels used to calibrate the Triton Canister System have…

Stryker Instruments Div. of Stryker Corporation recalls SafeAir Telescopic Smoke Evacuation Pencil, Product No. 0703 046 004. The product is a Bovie pencil that is 75 inches l…

January 13, 2020 · Medical device recalls Moderate risk Hairline fractures in a component could allow electrical current to arc out of…

Stryker Instruments Div. of Stryker Corporation recalls Telescopic Uncoated (Push Button), Product No. SHK TSPL. The product is a Bovie pencil that is 75 inches long compresse…

January 13, 2020 · Medical device recalls Moderate risk Hairline fractures in a component could allow electrical current to arc out of…

Stryker Instruments Div. of Stryker Corporation recalls Telescopic Smoke Evac Pencil, PB, Coated, Product No. SHKTSPCL. The product is a Bovie pencil that is 75 inches long co…

January 13, 2020 · Medical device recalls Moderate risk Hairline fractures in a component could allow electrical current to arc out of…

Stryker Instruments Div. of Stryker Corporation recalls Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 2PRT(Dual Port) Quick Connect Connector…

November 6, 2019 · Medical device recalls Moderate risk There is a potential for the cuff to leak air leading to a loss of vascular occ…

Stryker Instruments Div. of Stryker Corporation recalls Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 1PRT(Single Port) Quick Connect Connect…

November 6, 2019 · Medical device recalls Moderate risk There is a potential for the cuff to leak air leading to a loss of vascular occ…

Stryker Instruments Div. of Stryker Corporation recalls C2 Nerve Monitor, 8 Channel, 5140-508-280, UDI 07613327277319 Product Usage: The C2 Nerve Monitor System is intended fo…

July 31, 2019 · Medical device recalls Moderate risk Stryker C2 NerveMonitor's design and instructions may not optimally address usa…

Stryker Instruments Div. of Stryker Corporation recalls C2 Nerve Monitor, 4 Channel, 5140-508-240, UDI 07613327177329 Product Usage: The C2 Nerve Monitor System is intended fo…

July 31, 2019 · Medical device recalls Moderate risk Stryker C2 NerveMonitor's design and instructions may not optimally address usa…

Stryker Instruments Div. of Stryker Corporation recalls Performance Series Sagittal Blade, Catalog Number 6125-127-100 Product Usage: The Stryker Heavy Duty Sagittal Blades ar…

March 19, 2019 · Medical device recalls Moderate risk During manufacture, packaging materials for a small portion of the lot may not…

Stryker Instruments Div. of Stryker Corporation recalls Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6

December 4, 2018 · Medical device recalls Gauss Surgical is updating the Instructions for Use (IFU) for our Triton Sponge…

Stryker Instruments Div. of Stryker Corporation recalls T4 Zipper Toga (S/M); Catalog Number: 0400-810-000 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls T4 Zipper Toga, X-Large; Catalog number: 0400-850-000 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls T5 Zipper Toga with Peel-Away Face Shield, (XL/T); Catalog number: 0400-850-100 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls T4 Pullover Toga, L/XL; Catalog Number: 0400-720-000 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls T4 Zipper Toga, Regular; Catalog number: 0400-830-000 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls T4 Zipper Toga, (L/XL); Catalog Number: 0400-820-000 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls T4 Pullover Toga, X-Large; Catalog Number: 0400-770-000 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls T4 Pullover Toga, (S/M); Catalog Number: 0400-710-000 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls T4 Pullover Toga, Regular ; Catalog Number: 0400-750-000 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls T4 Pullover Toga, Large; Catalog Number: 0400-760-000 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls T5 Zipper Toga with Peel-Away Face Shield, (L/XL); Catalog number: 0400-820-100 Sterile personal protection garment

February 23, 2018 · Medical device recalls Moderate risk Separation of material layers may occur, causing a potential risk of exposure t…

Stryker Instruments Div. of Stryker Corporation recalls Revolution CMS w/ Femoral Breakaway Nozzle & Med. Press., Product Number: 0606-573-000, UDI: (01)4546540912114 for orth…

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls Intramedullary Brush Standard O.D. 14 mm, Product Number: 6198-001-514, UDI: (01)4546540255853 for orthopedic use.

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls PCD Kit: Long 90, 13g Match-Ground w/ Bevel, Product Number: 0506-485-000, UDI: (01)4546540907035 for spinal orthopedic…

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls 11g Verteport Cement Cannula (18/pkg), Product Number: 0306-511-000, UDI: (01)7613252594307 for spinal orthopedic use.

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls 10g/15mm (15/2) iVAS System Kit, Product Number: 0705-115-000, UDI: (01)7613252029830 for spinal orthopedic use.

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls 1. 11g/10mm iVAS System Kit, Product Number: 0705-310-000, UDI: (01)7613252505983; 2. 11g/15mm iVAS System Kit, Product…

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls Advanced Cement Mixing (ACM) Kit w/ Femoral Breakaway Nozzle & Prox. Med. Press., Product Number: 0306-573-000, UDI: (0…

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls 1. Femoral Canal Pressurizer without Hub, Medium, Blue, Product Number: 0206-546-000, UDI: (01)4546540039552; 2. Femora…

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls Break-Away Femoral Nozzle, Product Number: 0206-512-000, UDI: (01)4546540039415 for orthopedic use.

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls 1. AutoPlex System, Product Number: 0605-887-000, UDI: (01)4546540593108; 2. AutoPlex System: w/ VertaPlex HV, Product…

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls Revolution 90 Degree Tibial Nozzle, Product Number: 0606-516-000, UDI: (01)4546540911971 for orthopedic use.

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls 1. InterPulse Handpiece with coaxial bone cleaning tip, Product Number: 0210-110-100, UDI: (01)4546540861641; 2. InterP…

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls 180-Gram Cement Cartridge with Breakaway Femoral Nozzle, Product Number: 0206-530-000, UDI: (01)4546540857880 for ortho…

November 9, 2017 · Medical device recalls Moderate risk Lack of sterility assurance as bioburden levels were found to be higher than in…

Stryker Instruments Div. of Stryker Corporation recalls The Stryker Thoracic Pedicle Feeler 6002-350-000 is a smart instrument for remote control of the navigation software an…

October 16, 2017 · Medical device recalls Moderate risk Stryker Instruments and Stryker Leibinger GmbH & Co. KG are voluntarily recalli…

Stryker Instruments Div. of Stryker Corporation recalls Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is u…

March 10, 2017 · Medical device recalls Moderate risk Product shipped proximate to or past the expiration date listed on the product…

Stryker Instruments Div. of Stryker Corporation recalls Stryker SmartLife Large Aseptic Housing (7126-120-000)

February 28, 2017 · Medical device recalls Moderate risk Stryker Instruments issued a notice of correction for an update to cleaning pra…

Stryker Instruments Div. of Stryker Corporation recalls 8470-009-040 4.0MM Precision Round, 16CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offe…

November 30, 2016 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling specific lots of sterile MIS Tools…

Stryker Instruments Div. of Stryker Corporation recalls 8450-107-530 3.0MM Precision Match Head, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product…

November 30, 2016 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling specific lots of sterile MIS Tools…

Stryker Instruments Div. of Stryker Corporation recalls 8470-009-030 3.0MM Precision Round, 16CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offe…

November 30, 2016 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling specific lots of sterile MIS Tools…

Stryker Instruments Div. of Stryker Corporation recalls 8450-010-040 4.0MM Round, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is u…

November 30, 2016 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling specific lots of sterile MIS Tools…

Stryker Instruments Div. of Stryker Corporation recalls 8450-009-030 3.0MM Precision Round, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offe…

November 30, 2016 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling specific lots of sterile MIS Tools…

Stryker Instruments Div. of Stryker Corporation recalls 8450-107-525 2.5MM Precision Match Head, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product…

November 30, 2016 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling specific lots of sterile MIS Tools…

Stryker Instruments Div. of Stryker Corporation recalls 8450-009-040 4.0MM Precision Round, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offe…

November 30, 2016 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling specific lots of sterile MIS Tools…

Stryker Instruments Div. of Stryker Corporation recalls RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U

October 11, 2016 · Medical device recalls Stryker Instruments is voluntarily recalling the Care Instructions/Instructions…

Stryker Instruments Div. of Stryker Corporation recalls Sagittal Blade 18.0X0.97X90MM, Model Number: 6118-097-090 Product Usage: Heavy duty Sagittal Blades are used to cut bon…

August 17, 2016 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the Sagittal Blade 18.0X.97X90MM d…

Stryker Instruments Div. of Stryker Corporation recalls 120 V Neptune 3 Rover, Model Number: 0703-001-000

July 1, 2016 · Medical device recalls Moderate risk Stryker initiated a voluntary recall of the 120 V Neptune 3 Rover on 07/01/2016…

Stryker Instruments Div. of Stryker Corporation recalls 2.3MM Tapered Router, Product Number 5407-FA2-023 A router is a cutting accessory used in the following medical applica…

June 24, 2016 · Medical device recalls Moderate risk A variation in flute depth on the routers was observed. The variation in flute…

Stryker Instruments Div. of Stryker Corporation recalls 6.0mm Round Fluted Bur, Super Long

June 16, 2016 · Medical device recalls Moderate risk Stryker Instruments initiated a voluntary recall of specific lots of Round Flut…

Stryker Instruments Div. of Stryker Corporation recalls 5.0mm Round Fluted Bur, Super Long

June 16, 2016 · Medical device recalls Moderate risk Stryker Instruments initiated a voluntary recall of specific lots of Round Flut…

Stryker Instruments Div. of Stryker Corporation recalls Stryker AutoPlex System. Model Numbers 0607-687-000, 0605-887-000, 0605-687-000, and 0605-683-000. For bone cement. Str…

June 14, 2016 · Medical device recalls Moderate risk The Piston Head can become separated from the Delivery Piston, blocking the inj…

Stryker Instruments Div. of Stryker Corporation recalls Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Pneumatic System is a pneumatically operated surgical…

April 28, 2016 · Medical device recalls Moderate risk Due to the buildup of grease within the hose and motor, the product may require…

Stryker Instruments Div. of Stryker Corporation recalls Spetzler Claw Tip, Universal - 5450-800-311 Spetzler Open Angle Micro Claw Tip, Universal - 5450-800-313 The Spetzler C…

March 22, 2016 · Medical device recalls Moderate risk The Spetzler Claw Tip was packaged with the incorrect Tip Sleeve Assembly. The…

SurgiCounter scanner recalled over fire hazard

March 21, 2016 · Medical device recalls Moderate risk The affected scanner does not correctly interact with the SC360 software. When…

Stryker Instruments Div. of Stryker Corporation recalls (Stryker) AccuPlace Round Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for com…

February 4, 2016 · Medical device recalls Moderate risk During an evaluation of the product packaging, it was determined that there is…

Stryker Instruments Div. of Stryker Corporation recalls (Stryker) AccuPlace Straight Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for…

February 4, 2016 · Medical device recalls Moderate risk During an evaluation of the product packaging, it was determined that there is…

Stryker Instruments Div. of Stryker Corporation recalls 50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user with inserting a needle at a predetermined ang…

February 4, 2016 · Medical device recalls Moderate risk During an evaluation of the product packaging, it was determined that there is…

Stryker Instruments Div. of Stryker Corporation recalls 50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user with inserting a needle at a predetermined ang…

February 4, 2016 · Medical device recalls Moderate risk During an evaluation of the product packaging, it was determined that there is…

Stryker Instruments Div. of Stryker Corporation recalls Cournand Modified 2-PC 19G, 5.4cm or (Guidewire Introducer Needle) 20 units per case The Stryker Guidewire Introducer N…

November 23, 2015 · Medical device recalls Moderate risk The Guidewire Introducer Needle (0910-192-000) was shipped after the documented…

Stryker Instruments Div. of Stryker Corporation recalls Neptune 2 Waste Management System Docking Station (120V and 230V), New and Refurbished Product Usage: The Stryker Docki…

July 20, 2015 · Medical device recalls Moderate risk The Fluid Coupling Sleeve, a component within the Neptune Waste Management Syst…

Stryker Instruments Div. of Stryker Corporation recalls Stryker SelectCore Variable Throw Biopsy Device, 14G, 10CM Product Usage: The Stryker SelectCore Variable Throw Biopsy…

June 2, 2015 · Medical device recalls Moderate risk Stryker Instruments is recalling the Stryker SelectCore Variable Throw Biopsy D…

Stryker Instruments Div. of Stryker Corporation recalls 0702-001-350Q, Diverter Valve Assembly 0702-001-000, Neptune 2 Rover Ultra (120V) 0702-001-000R, Repair Neptune 2 Rover…

May 22, 2015 · Medical device recalls Moderate risk Stryker Instruments is initiating a recall of the Neptune 2 Waste Management Sy…

Stryker Instruments Div. of Stryker Corporation recalls 0210-312-000-Woundcare Replacement kit with soft tip; 0210-318-000; Woundcare Replacement with fan tip; 0210-318-100- W…

May 8, 2015 · Medical device recalls Moderate risk Potential sterility breach in the packaging.

Stryker Instruments Div. of Stryker Corporation recalls Navigation System II-Cart, 7700-100-000 with Articulated Arm Camera, 7700-103-001 and Articulated Arm Camera, 7700-103-…

May 4, 2015 · Medical device recalls Moderate risk Stryker initiated a device recall of the Navigation System II-Cart, Camera Arti…

Stryker Instruments Div. of Stryker Corporation recalls EliteCore Full Core Biopsy Device. EliteCore 18G, 20cm with and without HiLiter tip, 15 cm with and without HiLiter tip…

April 24, 2015 · Medical device recalls Moderate risk Potential for the device cannula to overthrow past the intended length.

Stryker Instruments Div. of Stryker Corporation recalls 3/16 in. Double Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved troca…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls 1/8 in. Double Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls 3/16 in. Round Drain with Trocar Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls 3/16 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar woun…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls 1/4 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls 1/4 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls 1/8 in. Trocar with Single Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls 1/8 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls Ambulating Bulb Ambulating Bulb: The Ambulating Bulb comprises four main components: the suction reservoir, the PVC tub…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls 1/4 in. Double Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls 3/16 in. Curved Trocar with Wound Drain Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved troca…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker Corporation recalls 1/4 in. Round Drain with Trocar Curved Trocar with Wound Drain/Double Trocar with Wound Drain: The curved trocar wound…

March 26, 2015 · Medical device recalls Moderate risk Stryker Instruments is voluntarily recalling the CBCII Wound Drains and Ambulat…

Stryker Instruments Div. of Stryker product recalled over sterility concerns

March 25, 2015 · Medical device recalls The Stryker Universal Battery Charger is not transmitting usage data to the Str…

System 6 Aseptic Housing recalled over sterility concerns

January 7, 2015 · Medical device recalls Moderate risk Stryker is recalling System 6 Aseptic Housing, due to a failed Continuous Bond…

Stryker Instruments Div. of Stryker Corporation recalls Flyte Togas are components of the Stryker Flyte System and are intended to be worn over any Stryker Flyte Helmet. This…

December 22, 2014 · Medical device recalls A single lot (11121171) of Flyte Toga Peel-away X-Large (catalog number 0408-83…

Stryker Instruments Div. of Stryker Corporation recalls The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging Cradles are designed to be used with the SurgiCou…

June 16, 2013 · Medical device recalls Moderate risk Faulty SurgiCounter Charging Cradle can prevent the scanner from charging or do…