Food Recall Check
Class I · High risk Terminated Initiated Dec 22, 2020 (6 years ago)

Food Club Garlic Powder recall

Recalled by B&G Foods North America, Inc · Parsippany, NJ, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

B&G Foods, Inc. has initiated a recall because their garlic powder mistakenly had bacon-flavored bits, which contain soy, an allergen undeclared on the garlic powder labels.

Undeclared allergen: Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Food Club Garlic Powder, 5.37 ounce bottles, 12 bottles per case. " Best 324A0 C By NOV 19 22 / Best 325A0 By NOV 20 22

Quantity: 1301 Cases

Food: Spices & seasonings

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.

Best 324A0 C By NOV 19 22 Best 325A0 B By NOV 20 22

Where it was sold

Florida Minnesota Texas Virginia

FDA's distribution note: The product was disturbed to the following states: TX, VA, FL, MN

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. 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
B&G Foods North America, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 22, 2020
In FDA report of
Jan 20, 2021
Terminated
Nov 2, 2021
FDA recall number
F-0203-2021 · event 87050
Official record
FDA enforcement report search

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