Recall archive / FDA device enforcement
Exeter V40 Cemented Hip (125mm) Stem, Part Number 0580-1-044 — FDA record Z-0651-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Dec 30, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Exeter V40 Cemented Hip (125mm) Stem, Part Number 0580-1-044
- Reason
- There is a potential label mix between certain lots of Exeter V40 Cemented Hip (125mm) Stem and Exeter V40 Cemented Hip (150mm) Stem.
- Classification
- Class II
- Recalling firm
- Howmedica Osteonics Corp.
- Quantity
- 59 devices
- Agency-reported status
- Terminated
- Source record identifier
- Z-0651-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | GTIN: 04546540509048; Lot G7900236 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
The product was distributed to the following US states: MI
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Feb 23, 2022
- Recall initiation date
- Dec 30, 2021
- Center classification date
- Feb 17, 2022
- Termination date
- Mar 14, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.