FDA Device recall Z-0078-2014
Natural-Knee¿ II Femoral Component
- FDA Device
- Class II
- terminated
- Published 2013-11-06
On 2013-11-06 the FDA classified a Class II recall of Natural-Knee¿ II 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-0078-2014 |
| 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
Natural-Knee¿ II Femoral Component
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:6212, 6307-00-006/051 |
|---|
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-0078-2014%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.