Peanut Butter Strawberry Jam White Bread, keep refrigerated, net wt. 6.5 oz., UPC 8 40152 47409 6.
Summary
The FDA issued a Class I for Peanut Butter Strawberry Jam White Bread, keep refrigerated, net wt. 6.5 oz., UP by A G Specialty Foods Inc. Reason: Potential contamination with Salmonella..
Details
Source
Food Recall
External ID
F-1303-2022
Action Date
2022-06-22
Status
Terminated
Category
food
Product Description
Peanut Butter Strawberry Jam White Bread, keep refrigerated, net wt. 6.5 oz., UPC 8 40152 47409 6.
Lot/Code Info: Best Thru dates: 05/16/2022-06/03/2022. Lot Codes from 129 to 141.
Quantity Affected: 2,421 Packs
Reason for Recall
Potential contamination with Salmonella.
Distribution
Distributed in OR and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-23
Company
Happy Valley, OR
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 175 food recalls issued in the same week, part of 204 food-related FDA actions this month.
A G Specialty Foods Inc has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (A G Specialty Foods Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does A G Specialty Foods Inc have FDA actions?
A G Specialty Foods Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1303-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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