Corin TriFit CF SIZE 7 — Class II medical device recall Z-1851-2021
Terminated recall by Corin Ltd, reported 2021-06-23, distributed nationwide. Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice ve
| Recall number | Z-1851-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Corin Ltd, Cirencester, United Kingdom |
| Recall initiated | 2021-05-06 |
| Classified | 2021-06-11 |
| Reported by FDA | 2021-06-23 |
| Terminated | 2023-07-05 |
| Distributed | Nationwide (US) |
| Quantity | 1 units |
| Reason classes | labeling |
| Lot numbers | 467881 |
| Model numbers | 6961007 |
Product
Corin TriFit CF SIZE 7, LATERALISED 127o, COMBINED FIXATION STEM, CEMENTLESS, REF 6961007. Hip prosthesis component.
Reason for recall
Units from one batch of TriFit TS size 2 stem were found to be labeled as a TriFit CF size 7 stem. And vice versa.
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-1851-2021. 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.