Brolite Chill Do 24 Recall: Salmonella Contamination Risk
Brolite recalls 50-lb paper bags of Chill Do 24 (whey, corn flour, l-cyste:ine, potassium bromate) due to potential Salmonella contamination. Consumers should check lot code 192B8004 for affected products.
Lower-risk recall
Product contained an ingredient which may be contaminated with Salmonella
Contact the company
What happened, in plain English
Brolite is recalling a specific type of 50-lb paper bag of Chill Do 24 food product because it may contain Salmonella bacteria. This contamination could cause food poisoning if the product is consumed. Read more at govinfonow.com/recall/18907-brolite-chill-do-24-recall-salmonella-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/18907-brolite-chill-do-24-recall-salmonella-contamination-risk · Updated October 6, 2026 · FDA enforcement record: FDA #F-1820-2018
Cite this page
“Brolite Chill Do 24 Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18907-brolite-chill-do-24-recall-salmonella-contamination-risk. Based on FDA recall #F-1820-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1820-2018%22&limit=1).
Why it’s dangerous
Salmonella bacteria can cause food poisoning with symptoms like diarrhea, fever, and abdominal cramps. The product may be contaminated during manufacturing or handling, leading to illness if eaten.
Who’s affected
Anyone who purchased or uses Chill Do 24 food products from Brolite. Those with weakened immune systems are at slightly higher risk of foodborne illness.
How to tell if you have this one
Check for the product name 'Chill Do 24' and lot code 192B8004 on the 50-lb paper bag packaging.
- Brand
Brolite- Category
Food
What to do — step by step
Check Product Label
Look for the lot code 192B8004 on the 50-lb paper bag of Chill Do 24.
Where it went and when
Where it was distributed
Distributed in New Jersey.
FDA distribution: “NJ” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New Jersey.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1820-2018 (July 18, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1820-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.