Reported Apr 29, 2026 · Ongoing
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Remel Europe Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Remel Europe Ltd. · Clipper Boulevard West · Dartford, N/A · N/A
Is this the product you have?
- Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
- Lot codes and dates
UDI-DI 05056080500270 lots 6172600617274161713936150168610776737663993766400378049737195923709358626613062534106260215622235062338596233858
- Amount recalled
- 117 US; 950 OUS
Where it was sold
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new salmonella recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.