Class II — TEKNIMED SAS
| Recalling firm | Teknimed |
|---|---|
| Registered facility | TEKNIMED SAS (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Incorrect expiry date. Product is labeled with expiry date 2027-02-28. The correct expiration date is 2025-02-28. |
| Product | HIGH V+ Spinal Cement System REF T040321K |
| Quantity | 236 systems |
| Distribution | Worldwide distribution - U.S. Nationwide distribution in the state of MS and the countries of Poland, Lithuania, Spain, Taiwan, South Africa, Israel. |
| Initiated | 2022-12-15 |
| Classified | 2023-02-06 |
| Recall number | Z-1099-2023 |
| 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 — TEKNIMED SAS (Z-1099-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91493/
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