Microbiologics recalls LYFO DISK products with specific catalog numbers due to potential failure to recover Campylobacter jejuni subsp. jejuni. Affected units may not function correctly.
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
Microbiologics is recalling LYFO DISK products that may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni. This could affect laboratory testing accuracy if the product is used in microbiology applications.
The LYFO DISK may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni. This could lead to inaccurate laboratory test results if the product is used in microbiology applications.
Laboratory users who purchased LYFO DISK with catalog number 0325L are likely affected. Those using the product for microbiology testing may be at risk of inaccurate results.
Check for catalog number 0325L on the LYFO DISK. Affected units have UDI-DI: 10845357006476 and lot numbers 325-120-5, 325-119-3, or 325-119-6.
Verify the catalog number and lot numbers listed in the recall notice to confirm if your LYFO DISK is affected.
The recall notice states that affected units may fail to recover the target microorganism, but it does not indicate that the product is unsafe for use. The hazard is limited to potential testing inaccuracies.
The recall record does not specify a remedy, so no action is required beyond checking if your product matches the affected details.
Check for catalog number 0325L, UDI-DI: 10845357006476, and lot numbers 325-120-5, 325-119-3, or 325-119-6.
We’ve drafted a message you can send Microbiologics to request your refund or repair — edit it as you like.
Subject: Recall Z-0986-2026 — Microbiologics Microbiologics Hello, I own a Microbiologics that is covered by recall Z-0986-2026 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.
