Microbiologics recalls KWIKSTIK P. venetum products (catalog 0794P/0794K) due to Aspergillus flavus contamination in specific lots. Affected items may pose health risks from mold exposure.
A complaint investigation showed that the bulk pellets (lot 794-142) were contaminated with Aspergillus flavus.
Microbiologics is recalling KWIKSTIK P. venetum products (2-pack and 6-pack catalog numbers) because mold contamination was found in the bulk pellets. This could lead to health issues from inhaling or touching the mold.
The bulk pellets were contaminated with Aspergillus flavus, a mold that can cause health problems if inhaled or touched. This mold may grow in the product over time, especially in warm, humid environments.
Owners of KWIKSTIK P. venetum products with catalog numbers 0794P (2-pack) or 0794K (6-pack) and specific lot numbers are affected. People using these products for gardening or indoor plants are most at risk due to potential mold exposure.
Check for catalog numbers 0794P (2-pack) or 0794K (6-pack) on the product packaging. Look for lot numbers 794-142-2, 794-142-3, or 794-142-4 on the product label.
Identify the catalog number and lot number on your KWIKSTIK P. venetum product to confirm if it is affected.
The recall is due to contamination with Aspergillus flavus in the bulk pellets, which could pose health risks from mold exposure.
Products with catalog numbers 0794P (2-pack) or 0794K (6-pack) and lot numbers 794-142-2, 794-142-3, or 794-142-4.
Check the product packaging for catalog numbers 0794P or 0794K and look for lot numbers 794-142-2, 794-142-3, or 794-142-4.
We’ve drafted a message you can send Microbiologics to request your refund or repair — edit it as you like.
Subject: Recall Z-0307-2024 — Microbiologics Microbiologics Hello, I own a Microbiologics that is covered by recall Z-0307-2024 from Microbiologics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.