BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Lot Recall of SeriScaffold surgical scaffold devices, Allergan

Product group Non-active implants - special implants
Reference 00176/13

The manufacturer Allergan informs about a recall of two lot numbers of SeriScaffold as certain devices may have been packaged in improperly sealed pouches.

Lot Recall of SeriScaffold surgical scaffold devices, Allergan , Download_VeroeffentlichtAm_EN PDF, 548KB, File does not meet accessibility standards