Recall archive / FDA device enforcement
32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032 — FDA record Z-0644-2022
Reported ongoing
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 21, 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
- 32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
- Reason
- There is a potential for the outer Tyvek lid to de-bond from the sealed package.
- Classification
- Class II
- Recalling firm
- Howmedica Osteonics Corp.
- Quantity
- 8 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0644-2022
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 | UDI: 07613327012842; Lot Number: 87327407 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Worldwide distribution - US Puerto Rico and the countries of Canada, and Malaysia.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Feb 23, 2022
- Recall initiation date
- Dec 21, 2021
- Center classification date
- Feb 16, 2022
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.