FDA Device recall Z-0784-2014
Zimmer Segmental Systems
- FDA Device
- Class II
- terminated
- Published 2014-01-29
On 2014-01-29 the FDA classified a Class II recall of Zimmer Segmental Systems by Zimmer, citing after evaluation of 13 complaints(0.4% rate) for hyper-extension of the Zimmer Segmental System, Zimmer is updating the related surgical technique and instructions for use to prov….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0784-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-12-19 |
| Published | 2014-01-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer |
| Distribution | US |
Product
Zimmer Segmental Systems; Polyethylene Inserts, Size C. Knee replacement.
Reason
After evaluation of 13 complaints(0.4% rate) for hyper-extension of the Zimmer Segmental System, Zimmer is updating the related surgical technique and instructions for use to provide additional instructions and patient conditions that may place excessive loading on the polyethylene insert.
Identifiers
| code_info | Part numbers 00-5850-013-95 |
|---|
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-0784-2014%22
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