Class II — Corin Ltd
| Recalling firm | Corin Group |
|---|---|
| Registered facility | View this company's 4 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Some of the devices did not pass fatigue testing. |
| Product | TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component. |
| Quantity | 1 |
| Distribution | Distribution was made to NJ. There was no military/government distribution. |
| Initiated | 2022-07-12 |
| Classified | 2022-08-31 |
| Terminated | 2026-05-04 |
| Recall number | Z-1667-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Corin Ltd (Z-1667-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90662/
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