FDAMarch 25, 2026device

Oxoid Agglutinating Sera, Salmonella 9-0 R30957301

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

remel europeremel

UPCs

05056080500270

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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