Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
All systems mentioned in the attached file that were delivered with an actuator for the FlexVision Monitor Ceiling Suspension in the period 2003 to May 201 1 are affected.
Allura Xper FD10 C : 722001
Allura Xper FD10 F : 722002
- Please check attachment for all AFFECTED PRODUCTS -