Every recall we track for TELEFLEX MEDICAL INC — 32 in all — plus the complaints and injury reports the public filed about them.
Teleflex recalls sterile and non-sterile breathing tubes with torn corrugated sections. Affected products include Teleflex Flex tube (Product #20011) and Smooth-Flo Flex with Double Swivel (Products #22511, #22512, #22552).
Gibeck Humid-Vent 2S Flex DC humidifiers with specific product numbers (17731, 17732, 19061, 19062, 19812) have reported torn corrugated breathing tubes. Consumers should check their product numbers against the list provided.
Arrow recalls specific Percutaneous Thrombolytic Device kits (PTD) with potential tip separation during use. Affected kits include models PT-12709-WC with certain lot numbers. Contact Arrow for details.
Arrow recalls Percutaneous Thrombolytic Device kits with PTD tip separation risk. Affected units include specific lot numbers and components. Stop using immediately if you own these kits.
Arrow recalls PT-45509 PTD Sets with components PT-45509-S6 and PT-45509-T due to reported tip separation during use. Affected units have specific lot numbers.
Arrow recalls PTD Set (PTD) kits with specific lot numbers due to reported tip separation during use. Affected units may cause injury during dialysis procedures.
Arrow recalls 5 Fr. X 65 cm Arrow-Trerotola PTD Kit (REF PT-65509-HFC) due to reported tip separation during use. Affected units include specific lot numbers and component codes.
Arrow recalls Percutaneous Thrombolytic Device kits with PTD tip separation risk. Affected kits include specific lot numbers and components. Stop using if you have the recalled model.
Arrow recalls specific Percutaneous Thrombolytic Device kits (PTD) with potential tip separation during use. Affected units include certain lot numbers and model codes. Stop using immediately if you own these kits.
Teleflex recalls Polaris laryngoscopes with cracks or breaks at the hinge due to customer reports. Models 44401-44403 with specific lots are affected. Stop using if you have these items.
Teleflex recalls sterile thoracic catheters due to lack of sterility assurance. Affected units may cause infections if used without proper sterility.
Teleflex Medical recalls Pleur-evac Thoracic Catheters (DTRC-20S) due to potential sterility issues. These catheters are used in surgical procedures for chest drainage and must be used within 30 days.
Teleflex Medical recalls Rusch Greenlite laryngoscopes with specific product codes due to risk of breaking at welded joints during use. Affected units include certain lot numbers from 2018-2019.
Teleflex Medical recalls Rusch Greenlite laryngoscopes with product code 004551002 and GTIN 14026704663115 due to potential breaking at welded joints during use.
Teleflex Medical recalls Rusch Greenlite laryngoscopes with specific product codes due to risk of breaking at welded joints during use, potentially causing injury during tracheal intubation procedures.
Teleflex Medical recalls Rusch Greenlite laryngoscopes with specific product codes due to potential breaking at welded joints during use, which could lead to injury during tracheal intubation procedures.
Teleflex Medical recalls Rusch Greenlite laryngoscopes with specific product codes due to risk of breaking at welded joints during use, potentially causing injury during tracheal intubation procedures.
Teleflex Medical recalls Rusch Greenlite laryngoscopes with specific product codes due to potential breaking at welded joints during use, which could lead to injury during tracheal intubation procedures.
Teleflex Medical recalls Rusch Greenlite laryngoscopes with specific product codes due to potential breaking at welded joints during use, which could lead to injury during tracheal intubation procedures.
Teleflex Medical recalls Pleur-Evac Adult-Ped Wet chest drainage devices (product code A-8000I) due to potential sterile packaging compromise. Affected units include specific lot numbers listed in the recall notice.
Teleflex Medical recalls Pleur-Evac Adult-Ped Wet chest drainage systems due to potential sterile packaging compromise. Affected units have specific lot numbers. Consumers should check their product details.
Teleflex recalls RUSCH LASERTUBE rubber tubes for possible laser guard foil detachment in moisture, risking exposure during surgery. Affected units include specific sizes and lot numbers for tracheal intubation use.
Teleflex Medical recalls disposable aortic punch devices (2.8mm to 6.0mm) due to potential packaging compromise affecting sterility. Affected units have specific model numbers and lot numbers listed in the recall.
Teleflex Medical recalls Pilling Aortic Punch 4.0mm Standard Tip (REF 353440) due to potential packaging compromise affecting sterility. Affected units sold with lot number 74B1500674.
Teleflex Medical recalls Rusch Greenlite Single-Use Metal Laryng: blades may break at welded joints during setup or patient use, causing injury. Affected units have specific product codes and lot numbers.
Teleflex Medical recalls Rusch Green: Single-use metal laryngoscope blades that may break at welded joints, causing injury during patient use. Affected items have specific product codes and lot numbers.
Teleflex Medical recalls Hudson RCI Comfort Flo Corrugated Humidification Systems with Remote Temperature Port (REF 2416) due to potential water flooding and circuit entry during high flow oxygen therapy. Affected units have specific lot numbers.
Teleflex Medical recalls Hudson RCI Comfort Flo humidification systems with specific lot numbers due to potential water flooding in high flow oxygen therapy.
Teleflex Medical recalls Hudson RCI Comfort Flo Corrugated Humidification System (REF 2415) due to potential water flooding in oxygen therapy. Affected units have specific lot numbers.
Teleflex Medical recalls Hudson RCI Comfort Flo humidification systems with specific lot numbers due to potential water flooding in the circuit during high flow oxygen therapy, which could cause damage.
Teleflex Medical recalls Sprotte lumbar puncture needles with specific batch numbers due to potential packaging issues that may compromise sterility. Affected units could pose infection risks during medical procedures.
Teleflex Medical recalls Sprotte lumbar puncture needles with specific batch numbers due to potential packaging issues that may compromise sterility. Affected users should contact Teleflex for details.
