TaperFit Stem — Class II medical device recall Z-1667-2022
Terminated recall by Corin Ltd, reported 2022-09-07, distributed in NJ. Some of the devices did not pass fatigue testing.
| Recall number | Z-1667-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Corin Ltd, Cirencester, United Kingdom |
| Recall initiated | 2022-07-12 |
| Classified | 2022-08-31 |
| Reported by FDA | 2022-09-07 |
| Terminated | 2026-05-04 |
| Distributed | NJ |
| Quantity | 1 |
| UPC / GTIN / UDI-DI | 05055343871065 |
| Lot numbers | 494754 |
| Model numbers | 588.3800 |
Product
TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component.
Reason for recall
Some of the devices did not pass fatigue testing.
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-1667-2022. 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.