CLASS I Food recall · Reported 20 Jan 2021 · FDA Enforcement Report

Food Club Garlic Powder recalled by B&G Foods North America

B&G Foods North America is recalling Food Club Garlic Powder, distributed in Florida, Minnesota, Texas, Virginia. The recall was initiated on 22 Dec 2020 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest 324A0 C By NOV 19 22 Best 325A0 B By NOV 20 22
Quantity recalled1301 Cases

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-0203-2021
FDA event ID
87050
Recalling firm
B&G Foods North America, Parsippany, NJ
Classification
Class I
Status
Terminated
Recall initiated
22 Dec 2020
FDA classified
12 Jan 2021
Reported
20 Jan 2021
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Soy
Product category
Spices

Timeline

22 Dec 2020Recall initiated by company
12 Jan 2021Classified by FDA+21 days
20 Jan 2021Published in enforcement report+8 days

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

Reason for recall

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.

Product as listed by the FDA

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

Where it was distributed

The product was disturbed to the following states: TX, VA, FL, MN

FloridaMinnesotaTexasVirginia

Questions about this recall

Why was it 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.

Which lots are affected?

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

Where was it sold?

The product was disturbed to the following states: TX, VA, FL, MN

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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