R.L. Schreiber Demi-Glace Brown Sauce Mix Recalled for E. coli Risk
R.L. Schreiber recalls 18 oz bags of Demi-Glace Brown Sauce Mix due to potential E. coli contamination in flour. Check your lot numbers.
Stop using this now
Product was manufactured using flour potentially contaminated with E. coli.
Contact the company
What happened, in plain English
R.L. Schreiber Inc is recalling R.L. SCHREIBER Demi-Glace Brown Sauce Mix because the flour used may be contaminated with E. coli. This is a Class I recall, indicating a serious health risk. The product was distributed only to Florida. Read more at govinfonow.com/recall/23884-r-l-schreiber-demi-glace-brown-sauce-mix-recalled-for.
Source Summary by GovInfoNow · govinfonow.com/recall/23884-r-l-schreiber-demi-glace-brown-sauce-mix-recalled-for · Updated October 9, 2026 · FDA enforcement record: FDA #F-0673-2017
Cite this page
“R.L. Schreiber Demi-Glace Brown Sauce Mix Recalled for E. coli Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23884-r-l-schreiber-demi-glace-brown-sauce-mix-recalled-for. Based on FDA recall #F-0673-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0673-2017%22&limit=1).
Why it’s dangerous
The hazard arises because the flour used in manufacturing was potentially contaminated with E. coli. Ingesting this bacteria can cause serious foodborne illness.
Who’s affected
Consumers in Florida who purchased R.L. SCHREIBER Demi-Glace Brown Sauce Mix are affected. Anyone who consumed the contaminated flour is at risk of E. coli infection.
How to tell if you have this one
Look for R.L. SCHREIBER Demi-Glace Brown Sauce Mix in an 18 oz (510 G) white plastic bag. Check the product code CFDEMIGB 1470 and Lot #6-098-158723 on the packaging.
- Brand
R.L. Schreiber- Category
Food
What to do — step by step
Stop consuming the product
Do not eat the sauce mix if you have the recalled lot number.
Discard or return the item
The record does not specify a remedy, so please discard the product or contact the manufacturer for instructions.
Where it went and when
Where it was distributed
Distributed in Florida.
FDA distribution: “Product was shipped to FL only.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- 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-0673-2017 (July 5, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0673-2017 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 9, 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.