BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action and recall for m2000rt, Abbott

2011.09.30

Product group In-vitro diagnostics
Reference 04267/11

Corrective action and recall of Abbott for m2000rt due to a software problem. Customers were informed about the problem. There will be a software update.

Corrective action and recall for m2000rt, Abbott , Download_VeroeffentlichtAm_EN PDF, 425KB, File does not meet accessibility standards