Teleflex recalls
Teleflex appears in 151 official U.S. recall notices indexed by RecallRadar.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382045
FDA Device · Class I · 2023-07-05 · Teleflex - Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506535
FDA Device · Class I · 2023-07-05 · Teleflex - Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506530
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082050
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382030
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080065
FDA Device · Class I · 2023-07-05 · Teleflex - Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781045
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080085
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 112080070
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380035
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382060
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380040
FDA Device · Class I · 2023-07-05 · Teleflex - RUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 112480040
FDA Device · Class I · 2023-07-05 · Teleflex - Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030
FDA Device · Class I · 2023-07-05 · Teleflex - Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504570
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382065
FDA Device · Class I · 2023-07-05 · Teleflex - Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180030
FDA Device · Class I · 2023-07-05 · Teleflex - Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 504555
FDA Device · Class I · 2023-07-05 · Teleflex - Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781065
FDA Device · Class I · 2023-07-05 · Teleflex - Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780060
FDA Device · Class I · 2023-07-05 · Teleflex - Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111781035
FDA Device · Class I · 2023-07-05 · Teleflex - Preformed AGT Oral Endotracheal Tube Murphy Eye, High Volume, Low Pressure Cuff, REF 111780055
FDA Device · Class I · 2023-07-05 · Teleflex - Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506545
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082075
FDA Device · Class I · 2023-07-05 · Teleflex - Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082070
FDA Device · Class I · 2023-07-05 · Teleflex - Flexi-Set Uncuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 506550
FDA Device · Class I · 2023-07-05 · Teleflex - Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF 170095
FDA Device · Class I · 2023-07-05 · Teleflex - Teleflex HORIZON Microclip Titanium Ligating Clips w/tape, REF 005200
FDA Device · Class II · 2023-06-07 · Teleflex - Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat, REF 4000
FDA Device · Class II · 2023-05-24 · Teleflex - Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal
FDA Device · Class II · 2023-02-01 · Teleflex - Endotracheal Tube labeled as the following: a. Flexi-Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal
FDA Device · Class II · 2023-02-01 · Teleflex - Endotracheal Tube labeled as the following: a. Endotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff
FDA Device · Class II · 2023-02-01 · Teleflex - Pilling Wecksorb Cylindrical Sponges
FDA Device · Class II · 2023-01-04 · Teleflex - Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116)
FDA Device · Class II · 2022-11-23 · Teleflex - Iso-Gard Filter S, with Expandi-Flex, REF: a) 19261, OUS only
FDA Device · Class I · 2022-10-26 · Teleflex - Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only
FDA Device · Class I · 2022-10-26 · Teleflex - Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only
FDA Device · Class I · 2022-10-26 · Teleflex - Filter + Catheter Mount, REF 191667-000100, OUS only
FDA Device · Class I · 2022-10-26 · Teleflex - Iso-Gard Filter S with Expandi-Flex/Elbow: a) REF 19012, OUS only, b) REF 19012T with Tethered Cap, OUS only
FDA Device · Class I · 2022-10-26 · Teleflex - Iso-Gard Filter S, REF : a) 19211, OUS only
FDA Device · Class I · 2022-10-26 · Teleflex - Bronchial One Lumen Tube - Left
FDA Device · Class II · 2015-08-26 · Teleflex - Bronchial One Lumen Tube - Right
FDA Device · Class II · 2015-08-26 · Teleflex - Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile
FDA Device · Class II · 2015-08-26 · Teleflex - Carlens Bronchial Double Lumen Tube Set (Left) Sterile
FDA Device · Class II · 2015-08-26 · Teleflex - Tracheopart Set (Left), Sterile
FDA Device · Class II · 2015-08-26 · Teleflex - Bronchial Double Lumen Tube Set (Right), Sterile
FDA Device · Class II · 2015-08-26 · Teleflex - White Bronchial Double Lumen Tube Set (Right) Sterile
FDA Device · Class II · 2015-08-26 · Teleflex - Tracheopart Set (Right), Sterile
FDA Device · Class II · 2015-08-26 · Teleflex - Bronchial Double Lumen Tube Set (Left), Sterile
FDA Device · Class II · 2015-08-26 · Teleflex - R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated…
FDA Device · Class II · 2015-02-25 · Teleflex