Recall Z-2177-2013— Leica Microsystems (Schweiz) Ag
Class II · Terminated
Class II FDA medical device recall by Leica Microsystems (Schweiz) Ag, initiated 2012-12-18, terminated 2017-04-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Surgical microscope The device is used to improve the visibility of objects through magnification and illumination and can be applied for observation and documentation and for human veterinary medical treatment.. Reason: The brake in the Z axis and/or brakes in the AB and C axes failed during installation..
- Recalling firm
- Leica Microsystems (Schweiz) Ag
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2012-12-18
- Terminated
- 2017-04-24
- Firm location
- Heerbrugg, N/A, Switzerland
Product description
Surgical microscope The device is used to improve the visibility of objects through magnification and illumination and can be applied for observation and documentation and for human veterinary medical treatment.
Reason for recall
The brake in the Z axis and/or brakes in the AB and C axes failed during installation.
Data sourced from openFDA. This site is unofficial and independent of the FDA.