FDA recall record

Bruce Foods THE ORIGINAL CHICKEN FRY MIX FROM THE MAKERS OF LOUISIANA recall — FDA F-3056-2015

Products may be contaminated with peanut protein.

Class IIclassification
F-3056-2015official record ID
Sep 2, 2015report date

Recall record at a glance

Official recordF-3056-2015
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBruce Foods Corporation
Report dateSep 2, 2015
Recall initiation dateJul 27, 2015
Quantity147 cases of 12 units
LocationSaint Martinville, LA, United States

Official product description

THE ORIGINAL CHICKEN FRY MIX FROM THE MAKERS OF LOUISIANA BRAND HOT SAUCE, NET WT. 9 oz. (255g), BRUCE FOODS CORPORATION, EL PASO, TEXAS, UPC 1760002733

Why the product was recalled

Products may be contaminated with peanut protein.

Distribution information

FL, TX, LA, KS, AL, IA, WA, MN, NY

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.