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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.
October 8, 2014Medical DevicesFDA
Teleflex Medical recalls Hudson RCI¿ Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only, Product Usage: To administer med
Hazard: The pediatric breathing circuits can crack prior to and during use.
September 24, 2014Medical DevicesFDA
Teleflex Medical recalls Rusch, Soft Rubber (Nelaton and Nelaton Robinson), Bladder Catheter, Sterile. These catheters are indicated for the r
Hazard: Misbranding: Although the product labeling identifies the catheters as "soft rubber," the Natural Rubber Latex caution statement was not printed on the product label.
August 13, 2014Medical DevicesFDA
Teleflex Medical recalls RUSCH Foley Urinary Catheter Insertion Tray with 10cc syringe, BZK Swabs, Sterile, Rx only, Teleflex Medical Product C
Hazard: Labeling error: The manufacturing date is the same as the expiration date. The manufacturing date is correct, however the expiration date incorrectly indicates that the product is expired.
August 6, 2014Medical DevicesFDA
Teleflex Medical recalls RUSCH, TruLite, One-Piece Disposable Laryngoscope Handle Blade Combination, Non-Sterile, Rx Only, Distributed by: Telefl
Hazard: There is a possibility the handle of the laryngoscope may heat up and melt the end cap.
August 6, 2014Medical DevicesFDA
Teleflex Medical recalls Emerald Fiberoptic Blade, Macintosh 4, Teleflex Medical. A rigid laryngoscope is a device used to examine and visualize
Hazard: Packaging Error: Customers have reported receiving incorrect product. The box labeling indicates the correct product MAC 4 but the contents are incorrect, Miller 4 blades.
July 30, 2014Medical DevicesFDA
Teleflex Medical recalls Hudson RCI, Breathing Circuit, Adult Single Limb (W/Connector, Adaptor, Y Piece), Rx Only, Single Patient Use. The Hudso
Hazard: The temperature probe does not properly connect to the temperature port.
July 30, 2014Medical DevicesFDA
Teleflex Medical recalls Hudson RCI, Breathing Circuit, Adult, Single Limb w/Heated Wire, [Respiratory Gas Humidifier, (Direct Patient Interface)
Hazard: The temperature probe does not properly connect to the temperature port.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Humidifier Adaptor, 040 Shelf Pak, French, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Humidifier Adaptor 040, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Adaptor, 040 Hum, International, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak 640 SW, 650 mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak 640 SW, 650 mL w/040 Adaptor, French, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak 640 SW, 650 mL w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak SW/EAU Sterile, 650 mL w/Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aqua 540 SW, 540 w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak 340 SW, 340, mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak 340 SW, 340, mL w/040 Adaptor, French, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak SW/EAU, Sterile, 340 mL, w/Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak 340 SW, 340, mL w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak 101 SW, 190, mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak 640 SW, 650, mL w/040 Adaptor, International, Teleflex Medical, respiratory gas humidifier adaptor .
Hazard: The seals of the adaptor packaging may be creased which may potentially affect packaging integrity.
July 16, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak 340 SW, 340, mL w/040 Adaptor, International, Teleflex Medical, respiratory gas humidifier adaptor .
Hazard: The seals of the respiratory gas humidifier adaptor packaging may be creased which may potentially affect packaging integrity.
July 2, 2014Medical DevicesFDA
Teleflex Medical recalls RUSCH, LaserTube (Rubber), Laser Resistant Tracheal Tube, cuffed, Teleflex Medical, Willy-Rusch, GmbH. A trachea
Hazard: Although the Natural Rubber Latex caution symbol is clearly displayed on the product label, the accompanying caution statement "Caution: This product contains Natural Rubber Latex which may cause Allergic Reactions" was not printed on the product label.
June 18, 2014Medical DevicesFDA
Teleflex Medical recalls Taut Operative Cholangiogram Catheter, 4.5FR (1.5mm) x 76cm To facilitate the introduction of contrast media into the
Hazard: Several complaints were received for the metal support tube missing from the cholangiogram catheter.
June 18, 2014Medical DevicesFDA
Teleflex Medical recalls RUSCH Easy Cath Coude Kit, 10 FR, Rx Only, Sterile, Distributed by: Teleflex Medical, Research Triangle Park, NC 27708.
Hazard: Product was packaged with a straight catheter rather than the correct coude (curved) catheter.
May 14, 2014Medical DevicesFDA
Teleflex Medical recalls Deknatel Teleflex Medical Silk Black Braided Silk Suture Nonabsorbable Surgical Suture U.S.P. Indicated for use in s
Hazard: Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.
May 14, 2014Medical DevicesFDA
Teleflex Medical recalls Deknatel Teleflex Medical Stainless Steel 2 (metric 5) Monofilament Stainless Steel Suture, Nonabsorbable Surgical Sutur
Hazard: Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.
May 14, 2014Medical DevicesFDA
Teleflex Medical recalls Bard Fixt Suture Braided Polyester, Rx Only, Teleflex Medical, Research Triangle Park, NC USA Assembled in Mexico. In
Hazard: Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.
May 14, 2014Medical DevicesFDA
Teleflex Medical recalls Fixt Suture Bonded Plus Violet Braided Polyglycolic Acid Coated Suture, Synthetic Absorbable Surgical Suture, Sterile, R
Hazard: Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.
May 14, 2014Medical DevicesFDA
Teleflex Medical recalls Teleflex Medical, Research Triangle Park, NC, Polypropylene, Rx Only, Sterile, Distributed by Boston Scientific, Natick
Hazard: Product does not meet minimum needle attachment strength requirements; thus, the needle can become detached from the suture during use.