FDA Device recall Z-0313-2022
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028
- FDA Device
- Class II
- ongoing
- Published 2021-12-08
On 2021-12-08 the FDA classified a Class II recall of 28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028 by Howmedica Osteonics, citing XXX.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0313-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2021-10-15 |
| Published | 2021-12-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Howmedica Osteonics |
| Distribution | PR |
Product
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028
Reason
XXX
Identifiers
| code_info | UDI number - (01) 07613327012996(17)261913(10); lot numbers - 86953401, 86953503 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0313-2022%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.