FDA Medical devices recall ·
KWIK-STIK, Quality control kit for culture media… recall
- Recall number
- Z-0876-2026
- Date
- (initiated November 13, 2025)
- Company / brand
- Microbiologics Inc
200 Cooper Ave N, Saint Cloud, MN, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 5 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
Why was it recalled?
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI-DI: 30845357020018; Lot Number: 818-111-7
Distribution
International distribution to the countries of UAE, China, Singapore, Kazakhstan,
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0876-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.