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TELEFLEX MEDICAL Recalls
236 recalls on record · July 25, 2012 to June 1, 2022 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 5, 2019Medical DevicesFDA
Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000080, REF 102004, SIZE I.D. mm 8,0
Hazard: The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
June 5, 2019Medical DevicesFDA
Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0
Hazard: The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
June 5, 2019Medical DevicesFDA
Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0
Hazard: The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
June 5, 2019Medical DevicesFDA
Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0
Hazard: The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
June 5, 2019Medical DevicesFDA
Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0
Hazard: The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
February 27, 2019Medical DevicesFDA
Teleflex Medical recalls Pilling COOLEY SUMP-SUCTION TUBE, REF 351547
Hazard: The internal tip is missing from the device, causing the device to not function as intended.
January 30, 2019Medical DevicesFDA
Teleflex Medical recalls Percuvance(R) Percutaneous Shaft 36cm, PCVSHL3 The Percutaneous Surgical System with 5mm attachments is indicated for
Hazard: There is potential for a piece of the distal tip on the Percuvance shaft to become deformed and possibly break off during use. If a piece did break off it could compromise the functionality and security of the tool tip. Should this occur during use, surgical intervention may be required.
January 30, 2019Medical DevicesFDA
Teleflex Medical recalls Percuvance(R) Percutaneous Shaft 29cm, PCVSH3 The Percutaneous Surgical System with 5mm attachments is indicated for
Hazard: There is potential for a piece of the distal tip on the Percuvance shaft to become deformed and possibly break off during use. If a piece did break off it could compromise the functionality and security of the tool tip. Should this occur during use, surgical intervention may be required.
April 4, 2018Medical DevicesFDA
Teleflex Medical recalls Teleflex MEDICAL WECK Visistat 35. Used for the external skin closure of lacerations.
Hazard: Some boxes are labeled as Visistat Wide devices, when in fact the contain Visistat Regular devices. The 6 individually packaged units within the boxes are correctly labeled.
March 7, 2018Medical DevicesFDA
Teleflex Medical recalls Rusch Greenlite MAC 1, Catalog Number 004551001. Used during tracheal intubation.
Hazard: The pouch may contain the incorrect Rusch Green Lite product size. Pouches that are labeled as containing RUSCH GREEN LITE MAC 1 may instead contain RUSCH GREEN LITE MAC 2.
November 15, 2017Medical DevicesFDA
Teleflex Medical recalls WECK(R) from TELEFLEX Auto Endo5(R), Automatic Hem-o-lok(R) Clip Applier, REF AE05ML (IPN010797) Rx ONLY, STERILE EO
Hazard: The product has a non-conformity that may cause clips to mislead, jam or fall out of the applier.
November 8, 2017Medical DevicesFDA
Teleflex Medical recalls Teleflex(R) Percuvance(TM) Percutaneous Surgical System, Components: (a) 5 mm Atraumatic Johans Grasper, Catalog Number
Hazard: Teleflex is recalling these products because the jaws of the tool tip may break, causing a fragment of the tool tip to fall off during use.
October 25, 2017Medical DevicesFDA
Teleflex Medical recalls Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable sur
Hazard: The knife handles slot depth is out of specification, so blades may not fit on the handles properly.
October 4, 2017Medical DevicesFDA
Teleflex Medical recalls Percuvance 29cm Shaft The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate so
Hazard: For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
October 4, 2017Medical DevicesFDA
Teleflex Medical recalls Percuvance Scissors Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to penet
Hazard: For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
October 4, 2017Medical DevicesFDA
Teleflex Medical recalls Percuvance Maryland Dissector Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the mean
Hazard: For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
October 4, 2017Medical DevicesFDA
Teleflex Medical recalls Percuvance Johans Grasper Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to
Hazard: For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
October 4, 2017Medical DevicesFDA
Teleflex Medical recalls Percuvance Clip Applier Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means to p
Hazard: For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
October 4, 2017Medical DevicesFDA
Teleflex Medical recalls Percuvance Gripper Grasper Tool Tip The Percutaneous Surgical System with 5mm attachments is indicated for the means t
Hazard: For some of the recalled products, the security of the connection between the shaft and the tool tip may be compromised. For certain other recalled lots of the products, the jaws of the tool tips may close abruptly.
October 4, 2017Medical DevicesFDA
Teleflex Medical recalls LMA(TM) MADgic(TM) Laryngo-Tracheal Mucosal Atomization Devices: (a) MAD600 MADgic, (b) MAD700 MADgic, (c) MAD720 MADg
Hazard: Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
June 21, 2017Medical DevicesFDA
Teleflex Medical recalls Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel an
Hazard: Product size listed on the labeling is incorrect.
June 14, 2017Medical DevicesFDA
Teleflex Medical recalls Hudson RCI, Pediatric Nasal Cannula, Non-Flared Prongs, Rx only,
Hazard: Incorrect labeling; the box label indicates Pediatric, the product insert indicates an Adult device.
May 31, 2017Medical DevicesFDA
Teleflex Medical recalls INFANT 20/BX, Sterile, Single use Product Usage: Catheter Connector/Accessory
Hazard: FDA Class II
May 31, 2017Medical DevicesFDA
Teleflex Medical recalls PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Hazard: Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
May 31, 2017Medical DevicesFDA
Teleflex Medical recalls PE CONNECTOR 3/8 Y 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Hazard: Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
May 31, 2017Medical DevicesFDA
Teleflex Medical recalls PE CONNECTOR 3/8 STRAIGHT 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Hazard: Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
May 24, 2017Medical DevicesFDA
Teleflex Medical recalls WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external sk
Hazard: Some boxes are labeled as containing Visistat Wide devices, when they in fact they contained Visistat Regular device.
April 26, 2017Medical DevicesFDA
Teleflex Medical recalls Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Hazard: Some of the individual unit packaging (pouches) may be missing the lot number an expiration date.
March 29, 2017Medical DevicesFDA
Teleflex Medical recalls Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a
Hazard: Labeling error
February 15, 2017Medical DevicesFDA
Teleflex Medical recalls Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A trachea
Hazard: Labeling inconsistency - units labeled with a 7mm tube may contain a size 6.5mm tube, and units labeled 7.5mm tube may contain a size 5.5mm tube.