BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for SHER-I-SWIV and SHER-I-BRONCH, Teleflex Medical

2009.08.25

Product group Surgical equipment/ Anaesthesia
Reference 02976/09

Teleflex Medical recalls SHER-I-SWIV and SHER-I-BRONCH (several Article- and lotnumbers) produced between 1. May 2004 and 31. May 2009. The tether attaching to the double swivel cap may break at the attachment points. Fragments may be inhaled unnoticed into the patient’s lung.

Recall for SHER-I-SWIV and SHER-I-BRONCH, Teleflex Medical , Download_VeroeffentlichtAm_EN PDF, 527KB, File does not meet accessibility standards

Use of cookies

Cookies help us to provide our services. By using our website you agree that we can use cookies. Read more about our Privacy Policy and visit the following link: Privacy Policy (only in German)

OK