BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for the NAVIX™ Access Devices, Xlumena Inc.

Product group Optics / Precision engineering - precision instruments for gastrointestinal and urological endoscopy and hysteroscopy
Reference 02269/13

The Xlumena Inc. recalls all lots of one Catalog no. of the NAVIX™ Access Devices from the market. Fractures can occur at the distal end of the catheter under load.

Recall for the NAVIX™ Access Devices, Xlumena Inc. , Download_VeroeffentlichtAm_EN PDF, 122KB, File does not meet accessibility standards