Remel recalls Oxoid Antimicrobial Susceptibility Discs (UK-made) with specific model and lot numbers due to out of specification. Consumers should check their product details to determine if affected.
Out of Specification
Remel is recalling Oxoid Antimicrobial Susceptibility Discs made in the UK because they are out of specification. This means the discs may not work properly for testing, which could lead to inaccurate results in medical or lab settings.
The discs are out of specification, meaning they may not provide accurate results for antimicrobial susceptibility testing. This could lead to incorrect treatment decisions in medical settings, but does not pose a direct physical risk to users.
Healthcare professionals and labs using these discs for antimicrobial testing are most likely affected. The risk is low as the discs are for lab use only and not a direct safety hazard.
Check for model CT0223B and lot numbers listed: 2341375, 2343397, 2394162, 2403210, 2438023, 2463120, 2408058, 2438086, 2457651, 2832507, 2840771, 2935065, 2958576, 2968037, and 2978564. These discs are made in the UK and are for prescription-only use.
Identify your model number and lot numbers to confirm if the disc is affected by this recall.
The discs are out of specification and may not provide accurate results, but they do not pose a direct physical risk to users.
Check your model and lot numbers against the list provided in the recall to determine if affected. If affected, contact Remel for further instructions.
Look for model CT0223B and lot numbers listed: 2341375, 2343397, 2394162, 2403210, 2438023, 2463120, 2408058, 2438086, 2457651, 2832507, 2840771, 2935065, 2958576, 2968037, and 2978564.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-2142-2021 — Remel Remel Hello, I own a Remel that is covered by recall Z-2142-2021 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.
