FDAClass IINovember 22, 2023

Kwikstik recall: Contamination

KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack)

Why was Kwikstik recalled?

A complaint investigation showed that the bulk pellets (lot 794-142) were contaminated with Aspergillus flavus.

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?

a) UDI/DI 20845357019169, Lot Numbers: 794-142-2, 794-142-4 b) UDI/DI 30845357019173, Lot Numbers: 794-142-3

Product
KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack)
Recalling firm
Microbiologics Inc
Quantity
13 units
Distribution
Worldwide distribution - US Nationwide and the countries of Italy, France, Turkey, Peru, Mexico.
Recall date
November 22, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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