BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Corrective action for all IMPAX systems from Agfa

Product group Radiological technology
Reference 00655/07

Agfa has issued an information concerning the potential that plans or/and images in IMPAX are assigned to the wrong patient. The corrective action consists in a software update for all concerned systems.

Corrective action for all IMPAX systems from Agfa , Download_VeroeffentlichtAm_EN PDF, 117KB, File does not meet accessibility standards