Recall Z-0876-2026— Microbiologics Inc
Class II · Ongoing
Class II FDA medical device recall by Microbiologics Inc, initiated 2025-11-13. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Microbiologics Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-11-13
- Firm location
- Saint Cloud, MN, United States
Product description
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
Reason for recall
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
Data sourced from openFDA. This site is unofficial and independent of the FDA.