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Remel Europe Ltd. recalls Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Recalled April 29, 2026 · FDA recall Z-1923-2026 · Remel Europe
Hazard
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. · FDA Class II
Units
117 US; 950 OUS
Sold at
Worldwide - US Nationwide distribution to the states of AL, CA, FL, IA, IL, IN, MI, MN, MO, NC, NE, OH, SD, TX, WA.
Description
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.
Product
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Manufacturer(s)
Remel Europe Ltd.
Made in
United Kingdom
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →