Class II — CORENTEC CO., LTD
| Recalling firm | Corentec Co., Ltd. |
|---|---|
| Registered facility | CORENTEC CO., LTD. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Due to unsupported 10 year expiration date. |
| Product | LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Tibial Insert |
| Quantity | 397 |
| Distribution | US Nationwide distribution in the states of AL, AZ, CA, MI, PA, TX. |
| Initiated | 2024-03-29 |
| Classified | 2024-05-31 |
| Recall number | Z-1934-2024 |
| 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 — CORENTEC CO., LTD (Z-1934-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94380/
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