BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall for Transseptal Guiding sheath, Baylis Medical

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00658/10

The manufacturer Baylis Medical Systems recalls Transseptal Guiding sheaths from the market. See also BfArM case number 0608/10. Advisory Notice is only available in German language.

Recall for Transseptal Guiding sheath, Baylis Medical , Download_VeroeffentlichtAm_EN PDF, 247KB, File does not meet accessibility standards