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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.
November 18, 2015Medical DevicesFDA
Teleflex Medical recalls R¿sch Flexi-Slip Endotracheal Tube Stylet with Soft Distal Tip, Sterile, Rx only, Teleflex Medical.
Hazard: Due to reports of the plastic coating of the stylet splitting and/or breaking off of the stylet.
August 26, 2015Medical DevicesFDA
Teleflex Medical recalls HUDSON RCI, Sheridan, SHER-I-SWIV and SHER-I-SWIV/FO Double Swivel, Rx Only, Sterile. Used temporarily to make rigid
Hazard: The double swivel connector may crack or separate on the endobronchial tube.
August 26, 2015Medical DevicesFDA
Teleflex Medical recalls HUDSON RCI, Sheridan SHER-I BRONCH Accessory Pack, Rx Only, Sterile. Used to aspirate liquids or semisolids from a p
Hazard: The double swivel connector may crack or separate on the endobronchial tube.
August 26, 2015Medical DevicesFDA
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.,
Hazard: The double swivel connector may crack or separate on the endobronchial tube.
August 26, 2015Medical DevicesFDA
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., R
Hazard: The double swivel connector may crack or separate on the endobronchial tube.
July 1, 2015Medical DevicesFDA
Teleflex Medical recalls Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual
Hazard: The intake port may be blocked which can cause the bag to fail to fill.
May 6, 2015Medical DevicesFDA
Teleflex Medical recalls Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier, Rx Only.
Hazard: Customer complaints were received of power to the unit ceasing and the display going blank.
April 15, 2015Medical DevicesFDA
Teleflex Medical recalls Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.
Hazard: Package contains incorrect sized unit: The adult sized S-1100-08LF product contains an infant sized chest drainage system.
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK 640 SW, 650ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connec
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK 340 SW, 340ML W/040 ADAPTOR, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connec
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls ADAPTOR, 040 HUM, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile wat
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK 640 SW, 650ML W/040 ADAPTOR, FREN. Product Usage: The Humidifier Adaptor is an accessory which allows connec
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK 640 SW, 650ML W/040 ADAPTOR, FREN. Product Usage: The Humidifier Adaptor is an accessory which allows connec
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK SW/EAU STERILE, 650 ML W/ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connect
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK 640 SW, 650ML W/040 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connection o
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUA 540 SW, 540 W/040 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connection of ste
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK 340 SW, 340, ML W/040, ADAPTOR, JAPA. Product Usage: The Humidifier Adaptor is an accessory which allows con
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK 340 SW, 340 ML W/040 ADAPTOR, FREN. Product Usage: The Humidifier Adaptor is an accessory which allows conne
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK SW/EAU STERILE, 340 ML W/ADAPTOR Product Usage: The Humidifier Adaptor is an accessory which allows connecti
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK 340 SW, 340 ML W/040B ADAPTOR, BRI Product Usage: The Humidifier Adaptor is an accessory which allows connec
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK 340 SW, 340 ML W/404 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connection
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls AQUAPAK 101 SW, 190ML W/040 ADAPTOR, JAPA Product Usage: The Humidifier Adaptor is an accessory which allows connect
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls Hudson RCI¿ Humidifier Adaptor, 040 contained in the following units: HUMIDIFIER ADAPTOR 040 Product Usage: The Humi
Hazard: The packages may contain foreign material (black particles).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls LMA (Laryngeal Mask Airway) Supreme (New Cuff) Size 5, Sterile, Single use, Product Usage: Achieve and maintain con
Hazard: The labelling of units from the affected lot indicates that it contains a size 5 LMA Supreme (New Cuff), but may contain a size 4 LMA Supreme (New Cuff).
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls Hudson RCI, Sheridan, Preformed Tracheal Tubes, Cuffed and Uncuffed, Rx Only, Sterile, Teleflex Medical.
Hazard: Labeling; The affected product packaging is incorrectly labeled as being a cuffed oral ET tube; The correct product labeling is uncuffed nasal ET tube.
February 18, 2015Medical DevicesFDA
Teleflex Medical recalls MAQUET, SERVO Humidifier 163, Rx Only, Inmed Mfg. Sdn Bhd. Catalog No: XKC01-06-8125-8, Model No. 01-06-8125-8. A he
Hazard: Defects: Cracks that may occur in the center of the corrugated flex tube of the 15 mm and 22 mm ISO female connector.
December 24, 2014Medical DevicesFDA
Teleflex Medical recalls WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended for use in procedures inv
Hazard: The manufacturing dates and expiration dates were transposed on the Tyvek label.
December 24, 2014Medical DevicesFDA
Teleflex Medical recalls Sheridan/CF Cuffed Tracheal Tube, Sterile, Rx only, Teleflex Medical, Research Triangle Park, NC 27708. Designed for
Hazard: Product Labeling; Units from the affected lot indicates that it contains a size 8mm tracheal tube but may contain a size 7.5mm tracheal tube.
December 10, 2014Medical DevicesFDA
Teleflex Medical recalls Aqauapak 728 SW, 760 ML W/028 Adaptor, Intl, Product No. 403728; Aqauapak 1028 SW, 1070 ML/W028 Adaptor, Intl, Product N
Hazard: Possibility that the nebulizer adaptor packaging may have open or weak seals which may affect the sterility of the adaptor.
December 10, 2014Medical DevicesFDA
Teleflex Medical recalls Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak Nebuliz
Hazard: Possibility that the nebulizer adaptor packaging may have open or weak seals which may affect the sterility of the adaptor.