smith&nephew OXINIUM Femoral Head 12/14 Taper — Class II medical device recall Z-1901-2024
Ongoing recall by Smith & Nephew Inc, reported 2024-06-05. Packaging contained the incorrect size of femoral head from what was displayed on the label.
| Recall number | Z-1901-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew Inc, Memphis, TN, United States |
| Recall initiated | 2024-04-24 |
| Classified | 2024-05-24 |
| Reported by FDA | 2024-06-05 |
| Countries outside the US | AU, DE, GB, JP, PT |
| Quantity | 23 packages |
| Reason classes | labeling |
| Lot numbers | 23FM03219, 23FM04184 |
| Model numbers | 71343204, 71343604 |
| Expiration dates | 2033-06-20 |
Product
smith&nephew OXINIUM Femoral Head 12/14 Taper, REF 71343204, 32 MM OD +4, Sterile; and smith&nephew, 12/14 Taper, REF 71343604, 36 MM M / +4
Reason for recall
Packaging contained the incorrect size of femoral head from what was displayed on the label.
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-1901-2024. 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.