Recall archive / FDA device enforcement
LAPAROSCOPIC GYN. Medical convenience kit. — FDA record Z-2254-2025
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 Jun 11, 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
- LAPAROSCOPIC GYN. Medical convenience kit.
- Reason
- CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- Classification
- Class II
- Recalling firm
- AVID Medical, Inc.
- Quantity
- 18 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2254-2025
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 | Model No. EURO011-08; UDI: 10809160414248; Kit Lot No. 1613056. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Domestic: CA, IL, MD, OH, PA, TX, WA.
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
- Aug 13, 2025
- Recall initiation date
- Jun 11, 2025
- Center classification date
- Aug 4, 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.