Acumedia recalls Campylobacter Blood Free Selective Medium (PN 7527A) due to incorrect expiration date labeling. This lab product may expire prematurely, but does not pose immediate health risks.
The product is labeled with an incorrect expiration date.
Acumedia is recalling a lab culture medium used for growing Campylobacter bacteria. The product has an incorrect expiration date label, which could lead to using expired media that might not work properly in lab tests.
The product has an incorrect expiration date label. This means the lab medium might expire before the intended date, potentially causing failed bacterial cultures or inaccurate test results. However, it does not pose a direct health risk to users.
Laboratory users who purchased Campylobacter Blood Free Selective Medium (PN 7527A) with lot number 110685B. Researchers and lab technicians using this medium for bacterial isolation are most at risk of inaccurate test results.
Check for the product name 'Campylobacter Blood Free Selective Medium', product number PN 7527A, and lot number 110685B. This lab product is used in laboratory settings for selective bacterial isolation.
Verify the expiration date on the label matches the intended date for the product.
Yes, the product is safe to use but may have expired earlier than intended due to the incorrect label. This could affect lab results but does not pose a health risk.
Check the expiration date on the label. If it's expired, discard it; otherwise, use it as normal for lab work.
The official recall does not mention a fix or remedy for the expiration date issue.
We’ve drafted a message you can send Acumedia to request your refund or repair — edit it as you like.
Subject: Recall Z-0284-2019 — Acumedia Acumedia Hello, I own a Acumedia that is covered by recall Z-0284-2019 from Acumedia. 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.
