B&G Foods North America, Inc 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. - F-0203-2021
🇺🇸 United States
TerminatedClass I
Company
B&G Foods North America, Inc
Product
Food Club Garlic Powder, 5.37 ounce bottles, 12 bottles per…
Recall date
December 22, 2020
Terminated
November 2, 2021
Source
FDA
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.
- Recall initiated
- Reported by source
- Recall terminated
Recalled products
Product description
UPC
Quantity
Lot / code information
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
Not published in this source record
1301 Cases
Best 324A0 C By NOV 19 22 Best 325A0 B By NOV 20 22
Distribution
The product was disturbed to the following states: TX
VA
FL
MN
Official source record
Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0203-2021
Event ID
87050
Status
Terminated
Classification
Class I
Company
B&G Foods North America, Inc
Product description
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
Reason
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.
Recall initiation date
December 22, 2020
Report date
January 20, 2021
Classification date
Not published in this source record
Termination date
November 2, 2021
Distribution pattern
The product was disturbed to the following states: TX, VA, FL, MN
UPC, lot, and code information
Best 324A0 C By NOV 19 22 Best 325A0 B By NOV 20 22
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
A map highlighting the states named in the source's distribution description.
Distributed
No data published
Shading reflects state-level totals only, as published by the source. It does not imply
county-level or point-level precision.
Distribution map
State
Distributed
Texas
1
Virginia
1
Florida
1
Minnesota
1
States shown are extracted from the source's free-text distribution description above; a narrative
description (e.g. "distributed nationwide") may not list individual states to extract.
View raw source data
-- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for
current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of November 2, 2021.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company
or product is unsafe beyond what the official source has published.
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