PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: November 22, 2023 Initiated: October 18, 2023 #Z-0307-2024

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Microbiologics Inc
Units Affected
13 units
Distribution
Worldwide distribution - US Nationwide and the countries of Italy, France, Turkey, Peru, Mexico.
Location
Saint Cloud, MN

Frequently Asked Questions

What product was recalled?
KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack). Recalled by Microbiologics Inc. Units affected: 13 units.
Why was this product recalled?
A complaint investigation showed that the bulk pellets (lot 794-142) were contaminated with Aspergillus flavus.
Which agency issued this recall?
This recall was issued by the FDA Devices on November 22, 2023. Severity: Moderate. Recall number: Z-0307-2024.