BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action and recall from Radiometer Medical for ABL700/800 analyzers

2005.08.19

Product group In-vitro diagnostics
Reference 01790/05

Corrective action and recall from Radiometer Medical for ABL700/800 analyzers because of a risk for false results due to leak currents. Customers were informed about the problem and how to avoid it. A new software will be developed.

Corrective action and recall from Radiometer Medical for ABL700/800 analyzers , Download_VeroeffentlichtAm_EN PDF, 147KB,