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Medical Device

Oxoid Agglutinating Sera, Salmonella 9-0 R30957301

Recall date: 2026-04-29 · Source: FDA_DEVICE
Brand / Firm
Remel Europe Ltd.
Product
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Reason for recall
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.
Units affected
117 US; 950 OUS
Description
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
View official recall notice →