FDA Device recall Z-2500-2020
Irix-C Forceps Inserter
- FDA Device
- Class II
- terminated
- Published 2020-07-15
On 2020-07-15 the FDA classified a Class II recall of Irix-C Forceps Inserter by Xtant Medical, citing the strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2500-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-05-12 |
| Published | 2020-07-15 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Xtant Medical |
| Distribution | AZ, TX, WV |
Product
Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591
Reason
The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld.
Identifiers
| code_info | LOT: XS1920458A |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2500-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.