BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action and recall from for the software of Olympus systems AU400, AQU640 and AU2700

Product group In-vitro diagnostics
Reference 01682/05

Corrective action and recall from Olympus for the software of Olympus systems AU400, AQU640 and AU2700 because under specific circumstances the automatic repeat run mode may cause a misreporting of the results. Customers were informed about the problem and how to avoid it. A new software will be developed.

Advisory Notice is only available in German language.

Corrective action and recall from for the software of Olympus systems AU400, AQU640 and AU2700 , Download_VeroeffentlichtAm_EN PDF, 37KB,