Remel recalls Campy CVA Medium 100/PK (lot R01272) due to low Campylobacter Jejuni recovery in testing. This may affect lab use. No remedy specified.
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
Remel is recalling Campy CVA Medium 100/PK (lot R01272) because lab tests showed low recovery of Campylobacter Jejuni. This could mean the medium isn't reliably detecting the bacteria, which is important for lab work.
The medium may not reliably detect Campylobacter Jejuni bacteria during lab testing. This could lead to inaccurate results if the bacteria aren't recovering properly from the medium.
Lab users who purchased Campy CVA Medium 100/PK (lot R01272) from the manufacturer. Those testing Campylobacter Jejuni may be at slightly higher risk if using this lot.
Check for the lot number R01272 on the packaging. The product expires January 12, 2026. This specific lot was identified in testing.
Look for the lot number R01272 on the packaging to confirm if your product is affected.
No, this is a lab product. The recall is for laboratory use only, not home use.
The recall record does not specify a remedy. Check the lot number to see if it's affected.
The recalled lot number is R01272, which expires January 12, 2026. Check the packaging for this lot number.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-1474-2026 — Remel Remel Hello, I own a Remel that is covered by recall Z-1474-2026 from Remel. 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.
