Exeter V40 Cemented Hip — Class II medical device recall Z-0652-2022
Terminated recall by Howmedica Osteonics Corp., reported 2022-02-23. There is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cem
| Recall number | Z-0652-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Howmedica Osteonics Corp., Mahwah, NJ, United States |
| Recall initiated | 2021-12-30 |
| Classified | 2022-02-17 |
| Reported by FDA | 2022-02-23 |
| Terminated | 2024-03-14 |
| Quantity | 58 devices |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 04546540153296 |
| Lot numbers | G7900352 |
| Model numbers | 0580-1-440 |
Product
Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
Reason for recall
There is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cemented Hip (150mm) Stem.
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-0652-2022. 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.