Summary
The FDA issued a Class I for GE Bakery, Cookie, Thumbprint, Peanut Butter, 12 Oz., Clam Shell by Giant Eagle. Reason: Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination..
Details
Source
Food Recall
External ID
F-1389-2022
Action Date
2022-07-13
Status
Terminated
Category
food
Product Description
GE Bakery, Cookie, Thumbprint, Peanut Butter, 12 Oz., Clam Shell
Lot/Code Info: GE 21968800000 Cookie 12 Thumbprint Peanut Butter
Quantity Affected: 11 Units
Reason for Recall
Products were made with Jiff Peanut Butter and have the potential for Salmonella Contamination.
Distribution
The product was distributed domestically to the following State: PA
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-23
Company
Pittsburgh, PA
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 53 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Giant Eagle has 11 FDA actions in our database, including 11 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 (Giant Eagle) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Giant Eagle have FDA actions?
Giant Eagle has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1389-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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