FDA Device recall Z-2241-2014
Apex Arc Hip Stem, Size 2, HA Coated
- FDA Device
- Class II
- terminated
- Published 2014-08-27
On 2014-08-27 the FDA classified a Class II recall of Apex Arc Hip Stem, Size 2, HA Coated by Omnilife Science, citing staining on hip implant.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2241-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-05-09 |
| Published | 2014-08-27 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Omnilife Science |
| Distribution | CA, FL, MA, NY, OK, TX, VA |
Product
Apex Arc Hip Stem, Size 2, HA Coated; Product Code: HC-21002-HA
Reason
Staining on hip implant.
Identifiers
| code_info | Lot: 17284 |
|---|
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-2241-2014%22
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