28MM -4 LFIT V40 HEAD — Class II medical device recall Z-0313-2022
Ongoing recall by Howmedica Osteonics Corp., reported 2021-12-08, distributed in PR. XXX
| Recall number | Z-0313-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Howmedica Osteonics Corp., Mahwah, NJ, United States |
| Recall initiated | 2021-10-15 |
| Classified | 2021-11-30 |
| Reported by FDA | 2021-12-08 |
| Distributed | PR |
| UPC / GTIN / UDI-DI | 07613327012996 |
| Lot numbers | 86953401, 86953503 |
| Model numbers | 6260-9-028 |
Product
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028
Reason for recall
XXX
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-0313-2022. 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.