Microbiologics Inc recalls KWIK-STIK 2-Pack
- Recalling company
- Microbiologics Inc
- Product
- KWIK-STIK 2-Pack, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325P
- Reason
- Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Dec 2, 2025
- Reported
- Dec 31, 2025
- Distribution
- Worldwide - US Nationwide.
- Status
- Ongoing
- Quantity
- 86 units (127 additional units 12/22/25)
- Lot / codes
- UDI-DI: 20845357006459; Lot Numbers: 325-120-3, 325-120-7, Additional Lots added 12/22/25: 325-119-1, 325-119-5
- Company location
- Saint Cloud, MN
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0984-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0984-2026 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.