Food Recall Check
Class II · Moderate risk Terminated Initiated Jul 21, 2017 (9 years ago)

BUSHS BEST¿ Country Style THICK recall

Recalled by Bush Brothers & Co · Knoxville, TN, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

During an FDA inspection the firm was informed that cans may have defective side seams which may cause the cans to leak or allow for growth of C. botulinum..

Pathogen: Botulism

Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

BUSHS BEST¿ Country Style THICK, RICH SAUCE WITH BACON & EXTRA BROWN SUGAR 28 OZ (1 LB 12 OZ) 794 g BUSH BROTHERS & COMPANY P. O. Box 52330, Dept, C KNOXVILLE, TN 37950-2330 UPC 0 39400 01974 9

Quantity: 5,979 cs/12/28 oz cans

Food: Sauces, dips & dressings

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot Codes 6077S RR, 6077P RR, 6087S RR, 6087P RR with the Best By date of Jun 2019

Where it was sold

Alabama Florida Georgia Indiana Kentucky Massachusetts Maine Michigan Missouri Mississippi North Carolina New York Ohio Pennsylvania Tennessee Texas Virginia

FDA's distribution note: Product was shipped to the following states: AL, FL, GA, IN, KY, MA, ME, MI, MO, MS, NC, NY, OH, PA, TN, TX & VA.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Bush Brothers & Co
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 21, 2017
In FDA report of
Aug 30, 2017
Terminated
Apr 5, 2018
FDA recall number
F-3404-2017 · event 77782
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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