Remel recalls Sensititre Gram Negative Susceptibility Testing Plates with potential lower than expected MICs for some gram-negative bacteria. Affected lots have specific expiration dates.
There are lower than expected MICs for some gram negative species.
Remel is recalling Sensititre Gram Negative Susceptibility Testing Plates due to possible lower than expected minimum inhibitory concentrations (MICs) for some gram-negative bacteria. This could lead to inaccurate antibiotic susceptibility testing results, which might affect treatment decisions.
The plates may show lower than expected minimum inhibitory concentrations (MICs) for certain gram-negative bacteria. This could cause inaccurate antibiotic susceptibility test results, potentially leading to incorrect treatment decisions if the testing is used for clinical purposes.
Laboratories using these testing plates for antibiotic susceptibility testing are affected. Researchers and clinical staff who rely on these plates for accurate bacterial resistance testing are most at risk.
Check for the product number MDRGN2F on the plate. Affected lots include B1402A (expires Oct 2022), B1315A (expires Aug 2022), B1211 (expires May 2022), B1161A (expires Apr 2022), B0361 (expires Aug 2021), and B0164B (expires Apr 2021).
Look for the lot numbers B1402A, B1315A, B1211, B1161A, B0361, or B0164B on the plate.
The product number is MDRGN2F.
Affected lots include B1402A (expires Oct 2022), B1315A (expires Aug 2022), B1211 (expires May 2022), B1161A (expires Apr 2022), B0361 (expires Aug 2021), and B0164B (expires Apr 2021).
The plates may have lower than expected minimum inhibitory concentrations for some gram-negative bacteria, which could lead to inaccurate antibiotic susceptibility test results.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-0722-2022 — Remel Remel Hello, I own a Remel that is covered by recall Z-0722-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
