Oxoid Agglutinating Sera recalled over Salmonella risk

Recall date

March 25, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Remel Europe Ltd. recalls Oxoid Agglutinating Sera, Salmonella 9-0 R30957301

Recall number

Z-1923-2026

FDA classification

Class II

Brand / firm

Remel Europe Ltd.

Sold / distributed

Worldwide - US Nationwide distribution to the states of AL, CA, FL, IA, IL, IN, MI, MN, MO, NC, NE, OH, SD, TX, WA.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Oxoid Agglutinating Sera, Salmonella 9-0 R30957301