FDA Device recall Z-0076-2014
Zimmer¿ Unicompartmental Knee Femoral Component
- FDA Device
- Class II
- terminated
- Published 2013-11-06
On 2013-11-06 the FDA classified a Class II recall of Zimmer¿ Unicompartmental Knee Femoral Component by Zimmer, citing the low density polyethylene (LDPE) bag used to package implants adheres to the highly polished surface of the devices.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0076-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-08-30 |
| Published | 2013-11-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer |
| Distribution | US |
Product
Zimmer¿ Unicompartmental Knee Femoral Component. Indicated for patients with painful and/or disabling knee joint.
Reason
The low density polyethylene (LDPE) bag used to package implants adheres to the highly polished surface of the devices.
Identifiers
| code_info | Part Number Range:00-5842-011/017-01/02 |
|---|
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-0076-2014%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.