Recall
FDAHealthMarch 25, 2026

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

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
March 25, 2026

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

What's affected?

Product
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Lot code
6172600

Additional details

UDI-DI 05056080500270 lots 6172600, 6172741, 6171393, 6150168, 6107767, 3766399, 3766400, 3780497, 3719592, 3709358, 6266130, 6253410, 6260215, 6222350, 6233859, 6233858

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 117 US; 950 OUS.

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.