FDA Device recall Z-2176-2013
Surgical microscope The device is used to improve the visibility of objects through magnification and illumination and can be applied for o…
- FDA Device
- Class II
- terminated
- Published 2013-09-18
On 2013-09-18 the FDA classified a Class II recall of Surgical microscope The device is used to improve the visibility of objects through magnification and illumination and can be applied for o… by Leica Microsystems Schweiz Ag, citing the brake in the Z axis and/or brakes in the AB and C axes failed during installation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2176-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-12-18 |
| Published | 2013-09-18 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Leica Microsystems Schweiz Ag |
| Distribution | US |
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.
Identifiers
| code_info | Serial Numbers: OH4-84712, OH4-84812, OH4-84912 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2176-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.