Corin METAFIX HIP STEM — Class II medical device recall Z-1509-2022
Ongoing recall by Corin Ltd, reported 2022-08-17, distributed nationwide. One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collar
| Recall number | Z-1509-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Corin Ltd, Cirencester, United Kingdom |
| Recall initiated | 2022-07-22 |
| Classified | 2022-08-09 |
| Reported by FDA | 2022-08-17 |
| Distributed | Nationwide (US) |
| Quantity | 5 devices |
| Lot numbers | 485630 |
| Model numbers | 579.0103 |
Product
Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103
Reason for recall
One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630.
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-1509-2022. 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.