Apex Arc Hip Stem — Class II medical device recall Z-2241-2014
Terminated recall by Omnilife Science Inc., reported 2014-08-27, distributed in CA, FL, MA, NY, OK, TX, VA. Staining on hip implant.
| Recall number | Z-2241-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Omnilife Science Inc., East Taunton, MA, United States |
| Recall initiated | 2014-05-09 |
| Classified | 2014-08-15 |
| Reported by FDA | 2014-08-27 |
| Terminated | 2014-08-19 |
| Distributed | CA, FL, MA, NY, OK, TX, VA |
| Quantity | 13 devices |
| Lot numbers | 17284 |
Product
Apex Arc Hip Stem, Size 2, HA Coated; Product Code: HC-21002-HA
Reason for recall
Staining on hip implant.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2241-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.