BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Recall of the Binax NOW Legionella Urinary Antigen 22 Test Kit from Binax

Product group In-vitro diagnostics
Reference 03162/06

Recall of Binax for the Binax NOW Legionella Urinary Antigen 22 Test Kit (lot number 024448) because of a packaging error. Customers were advised to replace the affected batch. The German market is not affected by the corrective action.

Recall of the Binax NOW Legionella Urinary Antigen 22 Test Kit from Binax , Download_VeroeffentlichtAm_EN PDF, 46KB, File does not meet accessibility standards