BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action from Siemens for Immulite® und Immulite® 1000 PSA Third Generation, Siemens

2013.09.24

Product group In-vitro diagnostics
Reference 04801/13

Corrective action from Siemens for Immulite® und Immulite® 1000 PSA 3. Generation due to calibration failure or erroneous quality controls. Customers were informed accordingly.

Corrective action from Siemens for Immulite® und Immulite® 1000 PSA Third Generation, Siemens , Download_VeroeffentlichtAm_EN PDF, 36KB, File does not meet accessibility standards