Recall archive / FDA device enforcement
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K — FDA record Z-0876-2026
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 13, 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
- KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
- Reason
- Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
- Classification
- Class II
- Recalling firm
- Microbiologics Inc
- Quantity
- 5 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0876-2026
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 | UDI-DI: 30845357020018; Lot Number: 818-111-7 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
International distribution to the countries of UAE, China, Singapore, Kazakhstan,
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Dec 10, 2025
- Recall initiation date
- Nov 13, 2025
- Center classification date
- Dec 2, 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.