Irix-C Forceps Inserter — Class II medical device recall Z-2500-2020
Terminated recall by XTANT Medical, reported 2020-07-15, distributed in AZ, TX, WV. The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsati
| Recall number | Z-2500-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | XTANT Medical, Belgrade, MT, United States |
| Recall initiated | 2020-05-12 |
| Classified | 2020-07-04 |
| Reported by FDA | 2020-07-15 |
| Terminated | 2021-03-19 |
| Distributed | AZ, TX, WV |
| Quantity | 4 units |
| Reason classes | device malfunction |
| Lot numbers | XS1920458A |
Product
Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591
Reason for recall
The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2500-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.