TELEFLEX Recalls
151 recalls on record · February 18, 2015 to July 8, 2026 · Medical Devices
Recalls by year
15
22
23
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170080
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170075
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170070
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170065
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170060
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170055
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
July 5, 2023Medical DevicesFDA
TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170050
Hazard: Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.
June 7, 2023Medical DevicesFDA
TELEFLEX LLC recalls Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200; for use in general surgical procedures that requi
Hazard: Teleflex LLC is initiating this voluntary field corrective action because the clip cartridges for the affected product is missing a key feature that restricts the application of the clip to the applier. With this step feature missing on the cartridge, the clip is mounted in a more variable position, allowing the clips to load farther back in the clip applier jaw grooves. This may potentially result in inappropriate or inadequate clip application to vascular structures.
May 24, 2023Medical DevicesFDA
TELEFLEX LLC recalls Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat, REF 4000; for sealing residual oozing of tissue tr
Hazard: The product contains an expired diluent vial. If the impacted product is used, the sterility of the diluent component cannot be assured as it has passed beyond the studied shelf life of the product.
February 1, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff;
Hazard: Potential for pilot balloon non-inflation or cuff non-deflation.
February 1, 2023Medical DevicesFDA
TELEFLEX LLC recalls Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal; b.
Hazard: Potential for pilot balloon non-inflation or cuff non-deflation.
February 1, 2023Medical DevicesFDA
TELEFLEX LLC recalls Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubat
Hazard: Potential for pilot balloon non-inflation or cuff non-deflation.
January 4, 2023Medical DevicesFDA
TELEFLEX LLC recalls Pilling Wecksorb Cylindrical Sponges
Hazard: Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.
November 23, 2022Medical DevicesFDA
TELEFLEX LLC recalls Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116).
Hazard: Product may not be sterile
October 26, 2022Medical DevicesFDA
TELEFLEX LLC recalls Filter + Catheter Mount, REF 191667-000100, OUS only. Catheter mount for circuit-patient connection (Endotracheal tube a
Hazard: Incidents of device splitting or detaching during use
October 26, 2022Medical DevicesFDA
TELEFLEX LLC recalls Iso-Gard Filter S with Expandi-Flex/Elbow: a) REF 19012, OUS only, b) REF 19012T with Tethered Cap, OUS only; Microbial
Hazard: Incidents of device splitting or detaching during use
October 26, 2022Medical DevicesFDA
TELEFLEX LLC recalls Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only; b) 19262T, OUS only; c) 19272T, OUS only;
Hazard: Incidents of device splitting or detaching during use
October 26, 2022Medical DevicesFDA
TELEFLEX LLC recalls Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-u
Hazard: Incidents of device splitting or detaching during use
October 26, 2022Medical DevicesFDA
TELEFLEX LLC recalls Iso-Gard Filter S, with Expandi-Flex, REF: a) 19261, OUS only; b) 19272, OUS only; Microbial medical gas filter, singl
Hazard: Incidents of device splitting or detaching during use
October 26, 2022Medical DevicesFDA
TELEFLEX LLC recalls Iso-Gard Filter S, REF : a) 19211, OUS only; b) 19212; Microbial medical gas filter, single-use. Bacterial/viral filte
Hazard: Incidents of device splitting or detaching during use
August 26, 2015Medical DevicesFDA
Teleflex, Inc. recalls Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile
Hazard: Customer complaints reporting that the cobb connector detached from the main connector prior to use.
August 26, 2015Medical DevicesFDA
Teleflex, Inc. recalls White Bronchial Double Lumen Tube Set (Right) Sterile
Hazard: Customer complaints reporting that the cobb connector detached from the main connector prior to use.
August 26, 2015Medical DevicesFDA
Teleflex, Inc. recalls Tracheopart Set (Right), Sterile
Hazard: Customer complaints reporting that the cobb connector detached from the main connector prior to use.
August 26, 2015Medical DevicesFDA
Teleflex, Inc. recalls Tracheopart Set (Left), Sterile
Hazard: Customer complaints reporting that the cobb connector detached from the main connector prior to use.
August 26, 2015Medical DevicesFDA
Teleflex, Inc. recalls Carlens Bronchial Double Lumen Tube Set (Left) Sterile
Hazard: Customer complaints reporting that the cobb connector detached from the main connector prior to use.
August 26, 2015Medical DevicesFDA
Teleflex, Inc. recalls Bronchial One Lumen Tube - Right
Hazard: Customer complaints reporting that the cobb connector detached from the main connector prior to use.
August 26, 2015Medical DevicesFDA
Teleflex, Inc. recalls Bronchial One Lumen Tube - Left
Hazard: Customer complaints reporting that the cobb connector detached from the main connector prior to use.
August 26, 2015Medical DevicesFDA
Teleflex, Inc. recalls Bronchial Double Lumen Tube Set (Right), Sterile
Hazard: Customer complaints reporting that the cobb connector detached from the main connector prior to use.
August 26, 2015Medical DevicesFDA
Teleflex, Inc. recalls Bronchial Double Lumen Tube Set (Left), Sterile
Hazard: Customer complaints reporting that the cobb connector detached from the main connector prior to use.
February 25, 2015Medical DevicesFDA
Teleflex, Inc. recalls R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation
Hazard: Teleflex Medical has issued an advisory notification for the RUSCH Curved Reinforced Endotracheal Tube because of a discrepancy between the labeled cuff diameter and the actual cuff diameter. The actual product cuff diameter meets required specification.