United StatesKWIK-STIK quality control kit for culture media (Vibrio parahaemolyticus derived from ATCC 17802), Catalog Number 0818K, UDI‑DI 30845357020018, Lot 818-111-7 (5 units) is affected; some of these units may have been packaged in pouches labeled as Lot 857-53-10. The recall was issued because products from Lot 818-111-7 may carry incorrect pouch labeling; affected units were distributed internationally to the UAE, China, Singapore and Kazakhstan.
What's being recalled
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
Recalling firm: Microbiologics Inc, Saint Cloud, MN, United States.
How to identify it
UDI-DI: 30845357020018; Lot Number: 818-111-7
The hazard
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
International distribution to the countries of UAE, China, Singapore, Kazakhstan,
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)