Remel recalls Oxoid Agglutinating Sera (Salmonella 9-0 R30957301) due to cross-reaction with 2-0 serotypes. Affected lots may misidentify Salmonella 9-O as 2-O, risking incorrect identification in lab tests.
Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a Salmonella 9-O serotype as a 2-O serotype.
Remel is recalling specific lots of Oxoid Agglutinating Sera for Salmonella 9-0 testing. The product may cross-react with 2-0 serotypes, leading to misidentification of Salmonella 9-O as 2-O in lab tests. This could cause incorrect results in food safety testing.
The recalled serum may cross-react with 2-0 serotypes within 60 seconds, causing it to misidentify Salmonella 9-O as 2-O. This error could lead to incorrect food safety test results if used in lab settings.
Laboratory users who test food for Salmonella 9-0 may be affected by the recalled lots. Those using the product for accurate serotyping are most at risk of misidentification.
Check for lot numbers 6172600, 6172741, 6171393, 6150168, 6107767, 3766399, 3766400, 3780497, 3719592, 3709358, 6266130, 6253410, 6260215, 6222350, 6233859, 6233858 on the Oxoid Agglutinating Sera product.
Look for the lot numbers listed in the recall: 6172600, 6172741, 6171393, 6150168, 6107767, 3766399, 3766400, 3780497, 3719592, 3709358, 6266130, 6253410, 6260215, 6222350, 6233859, 6233858.
The recalled Oxoid Agglutinating Sera may cross-react with 2-0 serotypes, causing misidentification of Salmonella 9-O as 2-O in lab tests.
Check the lot number on your product. If it matches the listed lots, stop using it and contact Remel for guidance.
No, the recall is for lab testing accuracy, not physical safety risks. The hazard is limited to potential misidentification in food safety tests.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-1923-2026 — Remel Remel Hello, I own a Remel that is covered by recall Z-1923-2026 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.
