Every recall we track for Teleflex Medical Europe Ltd — 11 in all — plus the complaints and injury reports the public filed about them.
RUSCH Flexi-Set Cuffed Endotracheal Tube and Stylet Set (REFs 504550-504590) recalled due to risk of cuff inflation while pilot balloon remains flat. Check lot numbers for affected units.
RUSCH Endotracheal Tubes with specific reference numbers may have a cuff that inflates while the pilot balloon remains flat. This could cause airway issues during medical procedures. Affected units include models 112080050-112080100 with listed lot numbers.
RUSCH Endotracheal Tubes with specific REF numbers and lot numbers may have a cuff that inflates while pilot balloon remains flat. This could cause airway issues during medical procedures. Affected units include models with REF numbers a) through k) and listed lot numbers.
RUSCH Slick Set Cuffed Endotracheal Tubes with specific REF and lot numbers recalled due to potential cuff inflation while pilot balloon remains flat.
Teleflex Medical Europe recalls universal surgical shears with handles that melt during sterilization. Affected lot numbers F7 and G7. Stop using immediately to prevent injury.
Teleflex Medical recalls Hudson RCI One Way Valve (REF 1644) due to potential disconnection causing ventilation interruption. Affected units sold in respiratory/anesthesia circuits.
Teleflex Medical recalls MAD700 laryngotracheal mucosal atomization device due to potential missing or incomplete package label information. Affected units may not have proper labeling for topical anesthetic use.
Teleflex Medical Europe recalls Baker Jejunostomy Tubes with latex that may cause allergic reactions. Check product codes and batch numbers for affected items.
Teleflex Medical Europe Ltd recalls latex rebreathing bags due to missing allergy warning. Check product codes and batch numbers for affected items. Contact for remedy.
Teleflex Medical Europe recalls rectal balloon catheters with latex that may cause allergic reactions. Affected units have specific batch numbers. Consumers should check packaging for the allergy warning.
Teleflex Medical recalls Simplastic suprapubic puncture instruments with latex that may cause allergic reactions. Affected products include specific model codes and batch numbers. Consumers should check packaging for the allergy warning.
