Remel recalls Mueller-Hinton Broth IVD (500g) due to potential incorrect cation labeling, which could lead to inaccurate lab test results. Affected lots: 1865331, expiring 06/2021.
Product may have incorrect cation information detailed on the product label.
Remel is recalling Mueller-Hinton Broth IVD (500g) because the product label might have incorrect cation information. This could cause lab tests to give inaccurate results if used without correction.
The product label might show incorrect cation information, which is critical for accurate bacterial culture testing. If the cations are wrong, lab results could be inaccurate, potentially leading to incorrect diagnoses or treatments.
Lab technicians and healthcare facilities using this specific broth for bacterial culture testing. Those who have the lot number 1865331 (expiring June 2021) are most at risk.
Check for the lot number 1865331 on the label. The product is a 500g Mueller-Hinton Broth IVD that makes 23.8 liters of culture medium, expiring June 2021.
Verify the cation details on the product label to ensure they match the correct specifications for accurate lab testing.
The recall is due to potential incorrect cation labeling, which could lead to inaccurate lab test results. It is not immediately dangerous but requires verification for accurate testing.
Check the lot number on the label. If it is 1865331 (expiring June 2021), you should verify the cation information to ensure accurate lab results.
Look for the lot number 1865331 on the label. The product is a 500g Mueller-Hinton Broth IVD that makes 23.8 liters, expiring June 2021.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-0209-2018 — Remel Remel Hello, I own a Remel that is covered by recall Z-0209-2018 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.
