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 | Ongoing |
| Reason | Potential for Unity CR Inserts Right size 6 from batch 529803 to be incorrectly labelled as Unity CR Inserts Right size 7 from batch 532405 and visa versa. |
| Product | Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthroplasty |
| Quantity | 1 units |
| Distribution | US: MI, TX, IL |
| Initiated | 2023-10-13 |
| Classified | 2023-11-02 |
| Recall number | Z-0214-2024 |
| 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-0214-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93144/
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