Microbiologics Inc recalls KWIK-STIK
- Recalling company
- Microbiologics Inc
- 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 – may cause temporary or medically reversible health consequences
- Recall date
- Nov 13, 2025
- Reported
- Dec 10, 2025
- Distribution
- International distribution to the countries of UAE, China, Singapore, Kazakhstan,
- Status
- Ongoing
- Quantity
- 5 units
- Lot / codes
- UDI-DI: 30845357020018; Lot Number: 818-111-7
- Company location
- Saint Cloud, MN
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0876-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0876-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.