BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of DakoCytomation for HercepTest

Product group In-vitro diagnostics
Reference 02525/05

Recall of DakoCytomation for HercepTest (lot number 00016943) and HercepTest for DakoCytomation Autostainer (lot number 00016965 and 00018107) due to a formulation error and a reduced staining intensity. Customers were informed to discard the affected batches.

Recall of DakoCytomation for HercepTest , Download_VeroeffentlichtAm_EN PDF, 114KB,