CLASS II Food recall · Reported 18 Apr 2018 · FDA Enforcement Report

Roast Beef Gravy Seasoning Manufacturer's recalled

Precise Food Ingredients is recalling Roast Beef Gravy Seasoning Manufacturer's, distributed in Texas. The recall was initiated on 14 Mar 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot numbers: WO25251 and WO25043
Quantity recalled896 pounds

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1010-2018
FDA event ID
79557
Recalling firm
Precise Food Ingredients, Carrollton, TX
Brand
Roast
Classification
Class II
Status
Terminated
Recall initiated
14 Mar 2018
FDA classified
12 Apr 2018
Reported
18 Apr 2018
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Sauces & Condiments

Timeline

14 Mar 2018Recall initiated by company
12 Apr 2018Classified by FDA+29 days
18 Apr 2018Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential for Salmonella contamination.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Roast Beef Gravy Seasoning Manufacturer's code: PF07040000 packaged in a multi-walled paper bag with poly liner, 28 pounds

Where it was distributed

Texas

Texas

Questions about this recall

Why was it recalled?

Potential for Salmonella contamination.

Which lots are affected?

Lot numbers: WO25251 and WO25043

Where was it sold?

Texas

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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