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Teleflex Medical Europe Recalls
11 recalls on record · April 18, 2018 to August 25, 2021 · Medical Devices
Recalls by year
18
21
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 25, 2021Medical DevicesFDA
Teleflex Medical Europe Ltd recalls RUSCH Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF numbers: a) 112082050 b) 112082055
Hazard: The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
August 25, 2021Medical DevicesFDA
Teleflex Medical Europe Ltd recalls RUSCH Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF numbers: a) 112080050 b) 112080055 c)
Hazard: The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
August 25, 2021Medical DevicesFDA
Teleflex Medical Europe Ltd recalls RUSCH Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 504550 b) 504555 c) 504560 d
Hazard: The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
August 25, 2021Medical DevicesFDA
Teleflex Medical Europe Ltd recalls RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170055 c) 170060 d) 1
Hazard: The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
July 4, 2018Medical DevicesFDA
Teleflex Medical Europe Ltd recalls Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general surgical scissors
Hazard: The incorrect plastic was used to manufacture the handles of these shears, which causes the handles to melt if sterilized.
May 9, 2018Medical DevicesFDA
Teleflex Medical Europe Ltd recalls Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the applica
Hazard: Teleflex Medical is recalling the affected product because there may be missing or incomplete information on the package label.
April 25, 2018Medical DevicesFDA
Teleflex Medical Europe Ltd recalls Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port, REF 1644, QTY 50 Product Usage: for use in resp
Hazard: These one-way valves may disconnect at the joint between the two components that make up the device, which would cause an interruption of ventilation to the patient.
April 18, 2018Medical DevicesFDA
Teleflex Medical Europe Ltd recalls Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b) 655500200 655520
Hazard: These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
April 18, 2018Medical DevicesFDA
Teleflex Medical Europe Ltd recalls Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551310 (b) 650704120
Hazard: These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
April 18, 2018Medical DevicesFDA
Teleflex Medical Europe Ltd recalls Rectal Catheters; Product Code Equivalent Code 580114 580114 Product Usage: Rectal Balloon Catheter i
Hazard: These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.
April 18, 2018Medical DevicesFDA
Teleflex Medical Europe Ltd recalls Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 (b) 153000005 153000005 (c) 153000010 1530
Hazard: These products contain latex, but the following statement is not included on any level of product packaging: Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.