Remel recalls specific lab culture media due to intermittent failure in stability testing with anaerobic microorganisms. Affected products include certain lot numbers and reference codes.
Products have intermittently failed performance testing during stability studies with various anaerobic microorganisms.
Remel is recalling specific lab culture media products that have shown intermittent failures in stability testing with anaerobic microorganisms. This could affect lab work involving these media if not properly handled.
These culture media products have occasionally failed stability tests when exposed to anaerobic microorganisms. This means they might not perform as expected in lab settings, potentially leading to inaccurate results.
Lab researchers and microbiologists using these specific culture media products are most at risk. The recall affects only the listed lot numbers and reference codes.
Check the product label for reference codes (e.g., REF 07182, REF 07180) and lot numbers (e.g., 258907, 259526). The affected products are only the specific ones listed in the recall notice.
Look for reference codes (e.g., REF 07182) and lot numbers (e.g., 258907) on the product label.
The recall indicates intermittent performance failures in stability testing, but the products are not unsafe for use. They may not perform as expected in lab settings.
Check the product label for reference codes (e.g., REF 07182) and lot numbers (e.g., 258907) listed in the recall notice.
The recall does not specify a remedy, so no action is required beyond checking the product label for affected codes.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-3017-2018 — Remel Remel Hello, I own a Remel that is covered by recall Z-3017-2018 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.
