Microbiologics recalls KWIK-STIK 6-Pack products that may fail to recover Campylobacter jejuni subsp. jejuni. Affected units have Catalog Number 0325K and specific lot numbers. No remedy is stated in the recall notice.
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
Microbiologics is recalling a 6-pack of KWIK-STIK products that may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni. This issue does not pose a direct risk to users but affects the product's intended function.
The recalled KWIK-STIK products may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni. This means the product does not work as intended for its purpose, but it does not pose a health risk to users.
Users of the KWIK-STIK 6-Pack with Catalog Number 0325K and specific lot numbers are affected. The risk is low as the product failure does not cause injury or harm.
Check for the Catalog Number 0325K on the product. Affected units have specific lot numbers: 325-120-1, 325-120-4, 325-120-6, and additional lots added on 12/22/25: 325-119-2.
Verify the Catalog Number 0325K and lot numbers listed in the recall notice to confirm if your product is affected.
No, the recall is for a failure in the product's intended function, not a safety hazard. The product does not pose a risk to users.
The recall notice does not specify any action steps. Check the product details to see if it matches the affected lot numbers.
Look for the Catalog Number 0325K and check if your lot number is one of: 325-120-1, 325-120-4, 325-120-6, or 325-119-2 (added on 12/22/25).
We’ve drafted a message you can send Microbiologics to request your refund or repair — edit it as you like.
Subject: Recall Z-0985-2026 — Microbiologics Microbiologics Hello, I own a Microbiologics that is covered by recall Z-0985-2026 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.
