BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of the CORDIS SV-5 and SV-8 Peripheral Steerable Guidewire

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02165/06

Cordis Corp. recalls certain lots of the CORDIS SV-5 and SV-8 Peripheral Steerable Guidewire from the market. The guidewires may have the potential for guidewire fracture resulting in tip separation.

Recall of the CORDIS SV-5 and SV-8 Peripheral Steerable Guidewire , Download_VeroeffentlichtAm_EN PDF, 83KB, File does not meet accessibility standards