Class II — XTANT Medical
| Recalling firm | Xtant Medical Holdings, Inc. |
|---|---|
| Registered facility | Xtant Medical Holdings, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld. |
| Product | Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591 |
| Quantity | 4 units |
| Distribution | AZ, TX and WV. |
| Initiated | 2020-05-12 |
| Classified | 2020-07-04 |
| Terminated | 2021-03-19 |
| Recall number | Z-2500-2020 |
| 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 — XTANT Medical (Z-2500-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85789/
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