FDA Device recall Z-0652-2022
Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
- FDA Device
- Class II
- terminated
- Published 2022-02-23
On 2022-02-23 the FDA classified a Class II recall of Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440 by Howmedica Osteonics, citing there is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cemented Hip (150mm) Stem.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0652-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-12-30 |
| Published | 2022-02-23 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Howmedica Osteonics |
| Distribution | MI |
Product
Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
Reason
There is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cemented Hip (150mm) Stem.
Identifiers
| code_info | GTIN: 04546540153296; Lot G7900352 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0652-2022%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.