Recall archive / FDA device enforcement
Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10. — FDA record Z-0926-2026
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 Nov 14, 2025. 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
- Halyard, GENERAL LAPAROSCOPY PACK. Catalog Number: VAST018-10.
- Reason
- Potential for incomplete seal on header bag.
- Classification
- Class II
- Recalling firm
- AVID Medical, Inc.
- Quantity
- 42 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0926-2026
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 | Catalog Number: VAST018-10. UDI-DI: 10809160452257. Lot Number: 1651776. Expiration Date: 3/12/2027 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US distribution to GA, IL, NE, MD.
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
- Dec 24, 2025
- Recall initiation date
- Nov 14, 2025
- Center classification date
- Dec 15, 2025
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.