Kwik-stik recall
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
Why was Kwik-stik recalled?
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI: 30845357020018; Lot Number: 818-111-7
- Product
- KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
- Recalling firm
- Microbiologics Inc
- Quantity
- 5 units
- Distribution
- International distribution to the countries of UAE, China, Singapore, Kazakhstan,
- Recall date
- December 10, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)