Every recall we track for Teleflex Medical — 46 in all — plus the complaints and injury reports the public filed about them.
Teleflex Medical recalls Hudson Sheridan Sheri-Bronch endobronchial tubes (REF 5-16135) due to incorrectly labeled tracheal and bronchial swivel connectors. This may cause confusion during medical procedures. Affected units were sold in specific lots.
Teleflex Medical recalls Arrow EZ-IO Intraosseous Vascular Access System 15mm Needle+Stabilizer Kit (Product Code 9018P-VC-005) due to safety cap dislodging, risking needle stick injuries and packaging contamination.
Teleflex Medical recalls Arrow EZ-IO Intraosseous Vascular Access System 45mm Needle+Stabilizer Kit (Product Code 9079P-VC-005) due to safety cap dislodging, risking needle stick injuries and packaging contamination.
Teleflex Medical recalls Arrow EZ-IO Intraosseous Vascular Access System 25mm Needle+Stabilizer Kit due to safety cap dislodging, risking needle stick injuries and packaging contamination.
WECK AutoEndo5 surgical clip appliers with model numbers listed may jam or misload, causing clips to fall out or break. Affected units include specific codes like 73J1600836. Contact WECK for details.
Teleflex Medical recalls WECK Hem-O-Lok AutoEndo5 5mm clip appliers due to misloading/jamming risks that could cause clips to fall out or break.
Teleflex Medical recalls Sheridan/CF Novaplus 7.0 mm tracheal tubes with specific batch numbers due to reported disconnections that may cause insufficient oxygenation.
Teleflex Medical recalls specific Sheridan/HVT Novaplus 15mm connectors (7.0-8.5mm) due to reported disconnections that could cause oxygen shortage requiring medical intervention.
Teleflex Medical recalls specific sizes of Sheridan LTS tracheal tubes due to reported disconnections causing oxygenation issues. Affected units include 4.0mm, 5.0mm, and 6.0mm models with listed batch numbers.
Teleflex Medical recalls Hudson RCI Sheridan Uncuffed tubes with specific sizes and batch numbers due to reported disconnections causing oxygenation issues. Affected units may require medical intervention.
Recalled Teleflex Medical Hudson RCI Sheridan Preformed tubes (3.0-9.0mm) may disconnect from breathing tubes, causing oxygenation issues. Check product references and batch numbers listed in the recall.
Teleflex Medical recalls Hudson RCI Sheridan/CF connectors (3.0-10.0mm) due to reported disconnections from breathing tubes, risking insufficient oxygenation. Affected units include specific batch numbers and reference codes.
Teleflex Medical recalls Hudson RCI Sheridan/HVT breathing tube connectors (5.0-10.0mm) due to reported disconnections causing oxygenation issues. Affected units have specific batch numbers listed in the recall.
Teleflex Medical recalls specific sizes of Sheridan EZ-ENDO connectors due to reported disconnections from breathing tubes, potentially causing insufficient oxygenation and requiring medical intervention.
Teleflex Medical recalls Rusch EasyCath Kit (ECK120 and ECK125) due to potential non-sterile condition. Affected units may pose infection risks during medical procedures.
Teleflex Medical recalls Hudson RCI Sheridan airway tubes with specific sizes and lot numbers due to reported disconnections from endotracheal tubes. This may cause breathing issues during medical procedures.
Teleflex Medical recalls Hudson RCI Sheridan airway connectors due to reported disconnections in specific lots. Affected products include 6.0mm to 8.5mm preformed connectors with listed product codes and lot numbers. This recall addresses a small reported issue in less than 0.0025% of distributed units.
Teleflex Medical recalls Novaplus 7.0-8.5mm Sheridan connectors due to reported disconnections from endotracheal tubes in specific lots. Affected products include model numbers V5-10314 to V5-10317 with listed lot numbers.
Teleflex Medical recalls Hudson RCI Sheridan LTS tracheal tubes with specific lot numbers due to reported connector disconnections. This may cause airway issues during medical procedures.
Teleflex Medical recalls Sheridan/CF Novaplus 7.0 mm tracheal tubes with specific lot numbers due to reported connector disconnections. Affected units may disconnect from endotracheal tubes during use.
Teleflex Medical recalls Hudson RCI Sheridan airway connectors with specific sizes and lot numbers due to reported disconnections. Check your product code and lot numbers to see if affected.
Teleflex Medical recalls Hudson RCI Sheridan 15mm connectors with specific sizes and lot numbers due to reported disconnections from endotracheal tubes. This voluntary recall addresses a small percentage of distributed products.
Teleflex Medical recalls Hudson RCI Sheridan EZ-ENDO tubes (6.0-8.5mm) due to reported disconnections from endotracheal tubes in rare cases. Affected lots listed in product details.
Teleflex Medical recalls Neonatal ConchaSmart Breathing Circuits with dual heated limbs due to reported cracks in swivel wye adaptors before use. This could lead to breathing gas delivery issues for infants.
Teleflex Medical recalls specific RUSCH LASERTUBE rubber products due to potential laser guard foil detachment. Affected units have specific lot numbers and sizes. No remedy provided in recall notice.
Teleflex Medical recalls RUSCH LASERTUBE (Rubber) with lot numbers 14151-18411 due to potential laser guard foil detachment. Affected units may have a risk of laser exposure.
Teleflex Medical recalls RUSCH LASERTUBE (Rubber) with laser guard foil that may partially separate at edges. Affected units have specific lot numbers and sizes.
Teleflex Medical recalls RUSCH LASERTUBE (Rubber) units with laser guard foil that partially separated at edges. Affected units have specific lot numbers and sizes. No remedy provided in official notice.
Teleflex Medical recalls RUSCH LASERTUBE (Rubber) units with laser guard foil that may partially separate at edges. Affected units include specific lot numbers and sizes. No remedy is stated in the recall notice.
Teleflex Medical recalls one-piece male external catheters with incorrect sterile labeling. The device is not meant to be sterile in normal use, but the label claims it is. Consumers should check product details and contact Teleflex for guidance.
Teleflex Medical recalls one piece male external catheters with incorrect sterile labeling. The device is not meant to be sterile in normal use for incontinence management.
Teleflex Medical recalls RUSCH CARE Premium Drain bags with missing UDI compliance labels. The labels do not affect device function but may cause issues with medical tracking.
Teleflex Medical recalls RUSCH 2000ml urinary drainage bags with non-compliant UDI labels. The missing UDI information does not affect device function but may cause regulatory issues.
Teleflex Medical recalls Pilling Sump-Suction Tube model REF 351547 with missing internal tip. This device may not function as intended. Affected units have lot numbers A8, C8, or I7.
Teleflex Medical recalls Visistat 35 devices where some boxes contain regular devices labeled as wide. This affects laceration closure products.
Teleflex Medical recalls Percuvance Percutaneous Shaft 29cm (PCVSH3) due to potential tip breakage during laparoscopic surgery, which may require surgical intervention.
Teleflex Medical recalls Percuvance 36cm surgical shafts with specific batch numbers due to potential tip breakage during laparoscopic procedures, requiring surgical intervention if broken.
