Teleflex Medical recalls

114 recalls on record · latest: October 30, 2019

Official U.S. recall history for Teleflex Medical, compiled from official government records.

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Teleflex Medical recalls HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product Usage: The Sheridan Endobronchial Tubes are i…

October 30, 2019 · Medical device recalls Moderate risk The tracheal and brochial swivel connectors are incorrectly labeled.

Teleflex Medical recalls Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit, Product Code 9001P-VC-005 - Product Usage:…

October 8, 2019 · Medical device recalls Moderate risk The safety cap attached to needles within the needle sets may become dislodged…

Teleflex Medical recalls Arrow EZ-IO Intraosseous Vascular Access System 45mm Needle+Stabilizer Kit, Product Code 9079P-VC-005 - Product Usage:…

October 8, 2019 · Medical device recalls Moderate risk The safety cap attached to needles within the needle sets may become dislodged…

Teleflex Medical recalls Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit, Product Code 9018P-VC-005 - Product Usage:…

October 8, 2019 · Medical device recalls Moderate risk The safety cap attached to needles within the needle sets may become dislodged…

Teleflex Medical recalls WECK Hem-O-Lok AutoEndo5, 5mm Automatic Endoscopie Hem-o-lok Applier, REF 543965 Automatic Endoscopic Surgical Ligating…

October 4, 2019 · Medical device recalls Moderate risk Certain clip appliers have an increase in misloading and/or jamming related com…

Teleflex Medical recalls WECK AutoEndo5, Automatic Hem-O-Lok Clip Applier, REF AE05ML Automatic Endoscopic Surgical Ligating Clip Appliers are d…

October 4, 2019 · Medical device recalls Moderate risk Certain clip appliers have an increase in misloading and/or jamming related com…

Teleflex Medical recalls Hudson RCI Sheridan EZ-ENDO: a) 5.0 mm, REF 5-22510 b) 5.5 mm, REF 5-22511 c) 7.0 mm, REF 5-22514 d) 7.5 mm, REF 5-2251…

July 30, 2019 · Medical device recalls High risk Reported complaints indicate an increased incidence of specific lots of the 15…

Teleflex Medical recalls Hudson RCI Sheridan/HVT: a) 5.0 mm, REF 5-10310 b) 5.5 mm, REF 5-10311 c) 6.0 mm, REF 5-10312 d) 6.5 mm, REF 5-10313 e)…

July 30, 2019 · Medical device recalls High risk Reported complaints indicate an increased incidence of specific lots of the 15…

Teleflex Medical recalls Hudson RCI Sheridan/CF: a) 3.0 mm, REF 5-10106, REF 5-10206 b) 3.5 mm, REF 5-10107 c) 4.0 mm, REF 5-10108, REF 5-10208…

July 30, 2019 · Medical device recalls High risk Reported complaints indicate an increased incidence of specific lots of the 15…

Teleflex Medical recalls Hudson RCI Sheridan Preformed: a) 3.0 mm, REF 5-22006, REF 5-22106 b) 3.5 mm, REF 5-22007, REF 5-22107 c) 4.0 mm, REF 5…

July 30, 2019 · Medical device recalls High risk Reported complaints indicate an increased incidence of specific lots of the 15…

Teleflex Medical recalls Hudson RCI Sheridan Uncuffed: a) 2.0 mm, REF 5-10404 b) 2.5 mm, REF 5-10405 c) 3.0 mm, REF 5-10406 d) 3.5 mm, REF 5-104…

July 30, 2019 · Medical device recalls High risk Reported complaints indicate an increased incidence of specific lots of the 15…

Teleflex Medical recalls Hudson RCI Sheridan LTS: a) 4.0 mm, REF 5-11108 b) 5.0 mm, REF 5-11110 c) 6.0 mm, REF 5-11112 Product Usage: Tracheal t…

July 30, 2019 · Medical device recalls High risk Reported complaints indicate an increased incidence of specific lots of the 15…

Teleflex Medical recalls Sheridan/HVT Novaplus: a) 7.0 mm, REF V5-10314 b) 7.5 mm, REF V5-10315 c) 8.0 mm, REF V5-10316 d) 8.5 mm, REF V5-10317…

July 30, 2019 · Medical device recalls High risk Reported complaints indicate an increased incidence of specific lots of the 15…

Teleflex Medical recalls Sheridan/CF Novaplus 7.0 mm, REF V5-10114 Product Usage: Tracheal tube/airway management

July 30, 2019 · Medical device recalls High risk Reported complaints indicate an increased incidence of specific lots of the 15…

Teleflex Medical recalls Rusch EasyCath Kit

July 1, 2019 · Medical device recalls Moderate risk Potential for product not to be sterile.

Teleflex Medical recalls Hudson RCI Sheridan: 1) EZ-ENDO 6.0 mm, Product Code 5-22512 2) EZ-ENDO 6.5 mm, Product Code 5-22513 3) EZ-ENDO 7.0 mm,…

May 24, 2019 · Medical device recalls High risk This voluntary recall is due to reported complaints (<0.0025% of all in scope d…

Teleflex Medical recalls Hudson RCI Sheridan: 1) CF 6.0 mm, Product Codes: 5-10112, 5-10212 2) CF 6.5 mm, Product Codes: 5-10113, 5-10213 3) CF…

May 24, 2019 · Medical device recalls High risk This voluntary recall is due to reported complaints (<0.0025% of all in scope d…

Teleflex Medical recalls Hudson RCI Sheridan: 1) HVT 6.0 mm, Product Code 5-10312 2) HVT 6.5 mm, Product Code 5-10313 3) HVT 7.0 mm, Product Cod…

May 24, 2019 · Medical device recalls High risk This voluntary recall is due to reported complaints (<0.0025% of all in scope d…

Teleflex Medical recalls Sheridan/CF Novaplus 7.0 mm, Product Code V5-10114 Product Usage: Tracheal tube/airway management

May 24, 2019 · Medical device recalls High risk This voluntary recall is due to reported complaints (<0.0025% of all in scope d…

Teleflex Medical recalls Hudson RCI Sheridan LTS, Product Code 5-11112 Product Usage: Tracheal tube/airway management

May 24, 2019 · Medical device recalls High risk This voluntary recall is due to reported complaints (<0.0025% of all in scope d…

Teleflex Medical recalls Sheridan/HVT: 1) Novaplus 7.0 mm, Product Code V5-10314 2) Novaplus 7.5 mm, Product Code V5-10315 3) Novaplus 8.0 mm, P…

May 24, 2019 · Medical device recalls High risk This voluntary recall is due to reported complaints (<0.0025% of all in scope d…

Teleflex Medical recalls Hudson RCI Sheridan: 1) Preformed 6.0 mm, Product Codes: a) 5-22212, b) 5-22312, c) 5-22112, d) 5-22012, 2) Preformed 6…

May 24, 2019 · Medical device recalls High risk This voluntary recall is due to reported complaints (<0.0025% of all in scope d…

Teleflex Medical recalls Hudson RCI Sheridan: 1) Uncuffed 6.0 mm, Product Code 5-10412 2) Uncuffed 6.5 mm, Product Code 5-10413 3) Uncuffed 7.0…

May 24, 2019 · Medical device recalls High risk This voluntary recall is due to reported complaints (<0.0025% of all in scope d…

Teleflex Medical recalls Teleflex HUDSON RDI NEONATAL ConchaSmart Breathing Circuit with Dual Heated Limb and ConchaSmart Column: a) REF 870-07K…

May 10, 2019 · Medical device recalls High risk Reported complaints of cracks being observed, prior to use, on swivel wye adapt…

Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0

April 1, 2019 · Medical device recalls Moderate risk The firm received reports indicating that the laser guard foil partially separa…

Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0

April 1, 2019 · Medical device recalls Moderate risk The firm received reports indicating that the laser guard foil partially separa…

Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0

April 1, 2019 · Medical device recalls Moderate risk The firm received reports indicating that the laser guard foil partially separa…

Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000080, REF 102004, SIZE I.D. mm 8,0

April 1, 2019 · Medical device recalls Moderate risk The firm received reports indicating that the laser guard foil partially separa…

Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0

April 1, 2019 · Medical device recalls Moderate risk The firm received reports indicating that the laser guard foil partially separa…

Teleflex Medical recalls Teleflex MEDICAL RuSCH One piece Male External Regular Catheter W/O Tape, REF A1500

February 27, 2019 · Medical device recalls The device label incorrectly states that the device is sterile. This product is…

Teleflex Medical recalls Teleflex MEDICAL RuSCH One piece Male External Medium Catheter W/O Tape, REF A1500M

February 27, 2019 · Medical device recalls The device label incorrectly states that the device is sterile. This product is…

Teleflex Medical recalls RUSCH Urinary Drainage bag, 2000mlm REF 390060 urine collection device

January 14, 2019 · Medical device recalls The device labels are not UDI compliant. The missing UDI compliance information…

Teleflex Medical recalls RUSCH CARE Premium Drain bag, 2000mlm REF 390000 urine collection device

January 14, 2019 · Medical device recalls The device labels are not UDI compliant. The missing UDI compliance information…

Teleflex Medical recalls Pilling COOLEY SUMP-SUCTION TUBE, REF 351547

January 7, 2019 · Medical device recalls Moderate risk The internal tip is missing from the device, causing the device to not function…

Teleflex MEDICAL WECK Visistat 35 recalled over laceration hazard

February 15, 2018 · Medical device recalls Moderate risk Some boxes are labeled as Visistat Wide devices, when in fact the contain Visis…

Teleflex Medical recalls Percuvance(R) Percutaneous Shaft 36cm, PCVSHL3 The Percutaneous Surgical System with 5mm attachments is indicated for t…

January 3, 2018 · Medical device recalls Moderate risk There is potential for a piece of the distal tip on the Percuvance shaft to bec…

Teleflex Medical recalls Percuvance(R) Percutaneous Shaft 29cm, PCVSH3 The Percutaneous Surgical System with 5mm attachments is indicated for th…

January 3, 2018 · Medical device recalls Moderate risk There is potential for a piece of the distal tip on the Percuvance shaft to bec…

Teleflex Medical recalls Teleflex(R) Percuvance(TM) Percutaneous Surgical System, Components: (a) 5 mm Atraumatic Johans Grasper, Catalog Number…

October 18, 2017 · Medical device recalls Moderate risk Teleflex is recalling these products because the jaws of the tool tip may break…

Teleflex Medical recalls WECK(R) from TELEFLEX Auto Endo5(R), Automatic Hem-o-lok(R) Clip Applier, REF AE05ML (IPN010797) Rx ONLY, STERILE EO

October 5, 2017 · Medical device recalls Moderate risk The product has a non-conformity that may cause clips to mislead, jam or fall o…

Teleflex Medical recalls Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means…

July 19, 2017 · Medical device recalls Moderate risk For some of the recalled products, the security of the connection between the s…

Teleflex Medical recalls Percuvance Gripper Grasper Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to…

July 19, 2017 · Medical device recalls Moderate risk For some of the recalled products, the security of the connection between the s…

Teleflex Medical recalls Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate sof…

July 19, 2017 · Medical device recalls Moderate risk For some of the recalled products, the security of the connection between the s…

Teleflex Medical recalls Percuvance Johans Grasper Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to…

July 19, 2017 · Medical device recalls Moderate risk For some of the recalled products, the security of the connection between the s…

Teleflex Medical recalls Percuvance Scissors Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetr…

July 19, 2017 · Medical device recalls Moderate risk For some of the recalled products, the security of the connection between the s…

Teleflex Medical recalls Percuvance Clip Applier Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to pe…

July 19, 2017 · Medical device recalls Moderate risk For some of the recalled products, the security of the connection between the s…

Teleflex Medical recalls LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720 MADgi…

July 5, 2017 · Medical device recalls Moderate risk Teleflex Medical is recalling the affected product because there may be missing…

Teleflex Medical recalls Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel a…

May 11, 2017 · Medical device recalls Moderate risk Product size listed on the labeling is incorrect.

Hudson RCI recalled over labeling errors

May 9, 2017 · Medical device recalls Moderate risk Incorrect labeling; the box label indicates Pediatric, the product insert ind…

Teleflex Medical recalls PE CONNECTOR 3/8 Y 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory

April 21, 2017 · Medical device recalls Moderate risk Labeling: The expiration date is not stated on the labeling, there is a potenti…

Teleflex Medical recalls PE CONNECTOR 3/8 STRAIGHT 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory

April 21, 2017 · Medical device recalls Moderate risk Labeling: The expiration date is not stated on the labeling, there is a potenti…

Teleflex Medical recalls PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory

April 21, 2017 · Medical device recalls Moderate risk Labeling: The expiration date is not stated on the labeling, there is a potenti…

Teleflex Medical recalls INFANT 20/BX, Sterile, Single use Product Usage: Catheter Connector/Accessory

April 21, 2017 · Medical device recalls Moderate risk

Teleflex Medical recalls Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.

March 29, 2017 · Medical device recalls Some of the individual unit packaging (pouches) may be missing the lot number a…

WECK Visistat 35R Disposable Skin Stapler recalled over laceration hazard

March 24, 2017 · Medical device recalls Moderate risk Some boxes are labeled as containing Visistat Wide devices, when they in fact t…

Teleflex Medical recalls Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a pa…

January 13, 2017 · Medical device recalls Moderate risk Labeling error

Teleflex Medical recalls Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.

January 10, 2017 · Medical device recalls Moderate risk The pouch may contain the incorrect Rusch Green Lite product size. Pouches that…

Teleflex Medical recalls RUSCH, Pocket PAC IC Intermittent Cath Kit, 8 FR, 12 FR, 14 FR, 10 FR and 16 FR, Rx Only, Sterile, Intermittent self-ca…

November 22, 2016 · Medical device recalls Moderate risk Labeling Inconsistency: The products have been labeled with the incorrect expir…

WECK Visistat 35W recalled over laceration hazard

November 18, 2016 · Medical device recalls Moderate risk Sterility Deficiency: The packages are not sealed properly and thus the sterili…

Teleflex Medical recalls Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous s…

November 16, 2016 · Medical device recalls Moderate risk The devices wings may become partially detached from the EFx Shield during use.

Teleflex Medical recalls ARROW OnControl Bone Marrow Biopsy System Tray, Sterile, Rx only, Manufactured for: Teleflex Medical, The Arrow OnContr…

November 8, 2016 · Medical device recalls Moderate risk Sterility: Due to a potential incomplete seal on the outer sterile package.

Teleflex Medical recalls ARROW OnControl Bone Lesion Biopsy System Tray, Sterile, Rx only, The Arrow OnControl Bone Lesion Biopsy System is inte…

November 8, 2016 · Medical device recalls Moderate risk Sterility: Due to a potential incomplete seal on the outer sterile package.

Teleflex Medical recalls OnControl Biopsy System Ported Needle Tray, Sterile, Rx only, The Arrow OnControl Bone Marrow Aspiration System is inte…

November 8, 2016 · Medical device recalls Moderate risk Sterility: Due to a potential incomplete seal on the outer sterile package.

Teleflex Medical recalls ARROW OnControl Bone Marrow Biopsy System Comprehensive Tray, Sterile, The Arrow OnControl Bone Marrow Aspiration Syste…

November 8, 2016 · Medical device recalls Moderate risk Sterility: Due to a potential incomplete seal on the outer sterile package.

Teleflex Medical recalls ARROW OnControl Ported Aspiration System Tray, Sterile, Rx only, The Arrow OnControl Bone Marrow Aspiration System is i…

November 8, 2016 · Medical device recalls Moderate risk Sterility: Due to a potential incomplete seal on the outer sterile package.

Teleflex Medical recalls Mucosal Atomization Device (MAD), Intranasal Mucosal Atomization Device with 3mL Syringe and Vial Adapter; Product Code…

October 27, 2016 · Medical device recalls Moderate risk Product Defect; These products may produce a straight stream instead of a fully…

Teleflex Medical recalls LMA MADomizer, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomized s…

October 27, 2016 · Medical device recalls Moderate risk Product Defect; These products may produce a straight stream instead of a fully…

Teleflex Medical recalls LMA MADdy, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray…

October 27, 2016 · Medical device recalls Moderate risk Product Defect; These products may produce a straight stream instead of a fully…

Teleflex Medical recalls LMA MADett, Endotracheal tube Mucosal Atomization Device, Rx only, Product Usage: These products are used for the deliv…

October 27, 2016 · Medical device recalls Moderate risk Product Defect; These products may produce a straight stream instead of a fully…

Teleflex Medical recalls FLEXI NOZZLE LONG, 10 Boxes of 25 units each Product Usage: These products are used for the delivery of topical anesthe…

October 27, 2016 · Medical device recalls Moderate risk Product Defect; These products may produce a straight stream instead of a fully…

Teleflex Medical recalls FLEXI NOZZLE SHORT Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray…

October 27, 2016 · Medical device recalls Moderate risk Product Defect; These products may produce a straight stream instead of a fully…

Teleflex Medical recalls LMA MADgic, Atomization Device with 3mL Syringe, Rx only, Product Usage: These products are used for the delivery of to…

October 27, 2016 · Medical device recalls Moderate risk Product Defect; These products may produce a straight stream instead of a fully…

Teleflex Medical recalls Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A trachea…

October 18, 2016 · Medical device recalls Moderate risk Labeling inconsistency - units labeled with a 7mm tube may contain a size 6.5mm…

Teleflex Medical recalls Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park,…

September 9, 2016 · Medical device recalls Moderate risk The product is being recalled due to a labeling error. The Gripper Graspers are…

Teleflex Medical recalls Teleflex Percuaneous Solutions, Johans Grasper, Ref ML004EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park,…

September 9, 2016 · Medical device recalls Moderate risk The product is being recalled due to a labeling error. The Gripper Graspers are…

Teleflex Medical recalls Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particularly in the case of a narrow tra…

August 26, 2016 · Medical device recalls High risk The connector may disconnect from the tracheostomy tube during use.

WECK¿ Horizon Manual-Load Ligating Clip Applier recalled over labeling errors

August 24, 2016 · Medical device recalls Moderate risk Misbranded: Incorrect etching on the device.

Teleflex Medical recalls Sterile Sheridan/HVT Cuffed, Murphy Eye, Tracheal Tube, Ref: V5-10314, ID: 7.0 mm, Rx Only, Manufactured by: Teleflex I…

May 5, 2016 · Medical device recalls Moderate risk The labeling of some units indicates that it contains a size 7mm tracheal tube,…

Teleflex Medical recalls Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product Usa…

March 30, 2016 · Medical device recalls Moderate risk The label on the Tyvek bag is missing. This is used by customers to identify ma…

Teleflex Medical recalls Weck EFx Classic Fascial Closure System, Rx Only, Sterile, The product is intended to facilitate placement and withdraw…

March 24, 2016 · Medical device recalls Moderate risk Incorrect expiration date was printed on the product label.

Teleflex Medical recalls Auto Endo5 Hem-o-lok Automatic Clip Applier, Medium Large Polymer Clips, Rx Only, Sterile, REF 543965 Product Usage: Th…

February 2, 2016 · Medical device recalls Moderate risk The clip in the applier may be missing a boss. A boss is the part of the clip t…

Teleflex Medical recalls Servo Humidifier 163, Model 01-06-8125-8, REF 6419365 Product Usage: A heat and moisture condenser (artifical nose) is…

December 3, 2015 · Medical device recalls Moderate risk Cracks may occur at the 15mm and 22mm ISO female connector.

Teleflex Medical recalls MAQUET Servo Humidifier 163, Inmed Mfg. Sdn. Bhd. Lot PT 2577, Jalan Perusahaan, 4, 34600 Kamunting, Perak, Malaysia.

December 3, 2015 · Medical device recalls Moderate risk Cracking may occur at the 15mm and 22mm ISO female connector.

Teleflex Medical recalls Taut Intraducers 10/BX7.5 FR 3.5, Product Code PI-93. To provide an access port into the peritoneal cavity.

October 14, 2015 · Medical device recalls Moderate risk The defective component can cause gas leakage through the device. This can resu…

Teleflex Medical recalls Rusch Flexi-slip tracheal tube Stylet, Size Ch 6, Sterile, Teleflex Medical.

August 24, 2015 · Medical device recalls Moderate risk Due to reports of the plastic coating of the stylet splitting and/or breaking o…

Teleflex Medical recalls R¿sch Flexi-Slip Endotracheal Tube Stylet with Soft Distal Tip, Sterile, Rx only, Teleflex Medical.

August 24, 2015 · Medical device recalls Moderate risk Due to reports of the plastic coating of the stylet splitting and/or breaking o…

Teleflex Medical recalls HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Right sided), Sizes: 28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr.,…

June 1, 2015 · Medical device recalls High risk The double swivel connector may crack or separate on the endobronchial tube.

Teleflex Medical recalls HUDSON RCI, Sheridan SHER-I BRONCH Accessory Pack, Rx Only, Sterile. Used to aspirate liquids or semisolids from a pati…

June 1, 2015 · Medical device recalls High risk The double swivel connector may crack or separate on the endobronchial tube.

Teleflex Medical recalls HUDSON RCI, Sheridan, SHER-I-SWIV and SHER-I-SWIV/FO Double Swivel, Rx Only, Sterile. Used temporarily to make rigid a…

June 1, 2015 · Medical device recalls High risk The double swivel connector may crack or separate on the endobronchial tube.

Teleflex Medical recalls HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Left sided), Sizes: 28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr.,…

June 1, 2015 · Medical device recalls High risk The double swivel connector may crack or separate on the endobronchial tube.

Teleflex Medical recalls Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual resu…

May 14, 2015 · Medical device recalls High risk The intake port may be blocked which can cause the bag to fail to fill.

Teleflex Medical recalls Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier, Rx Only.

April 1, 2015 · Medical device recalls Moderate risk Customer complaints were received of power to the unit ceasing and the display…

Teleflex Medical recalls Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.

March 13, 2015 · Medical device recalls Moderate risk Package contains incorrect sized unit: The adult sized S-1100-08LF product cont…

AQUAPAK 640 SW recalled over foreign material

January 14, 2015 · Medical device recalls Moderate risk The packages may contain foreign material (black particles).

AQUAPAK 340 SW recalled over foreign material

January 14, 2015 · Medical device recalls Moderate risk The packages may contain foreign material (black particles).

AQUAPAK 340 SW recalled over foreign material

January 14, 2015 · Medical device recalls Moderate risk The packages may contain foreign material (black particles).

Teleflex Medical product recalled over foreign material

January 14, 2015 · Medical device recalls Moderate risk The packages may contain foreign material (black particles).

AQUAPAK 101 SW recalled over foreign material

January 14, 2015 · Medical device recalls Moderate risk The packages may contain foreign material (black particles).

ADAPTOR recalled over foreign material

January 14, 2015 · Medical device recalls Moderate risk The packages may contain foreign material (black particles).

AQUAPAK SW/EAU STERILE recalled over foreign material

January 14, 2015 · Medical device recalls Moderate risk The packages may contain foreign material (black particles).

AQUAPAK 640 SW recalled over foreign material

January 14, 2015 · Medical device recalls Moderate risk The packages may contain foreign material (black particles).