Stonewall Kitchen brand Peanut Butter Maltballs packaged in 6oz clear plastic packaging
Summary
The FDA issued a Class I for Stonewall Kitchen brand Peanut Butter Maltballs packaged in 6oz clear plastic pa by Stonewall Kitchen, LLC. Reason: Product may contain undeclared peanut, soy, and wheat..
Details
Source
Food Recall
External ID
F-1476-2023
Action Date
2023-09-06
Status
Terminated
Category
food
Product Description
Stonewall Kitchen brand Peanut Butter Maltballs packaged in 6oz clear plastic packaging
Lot/Code Info: DEC31 2024
Quantity Affected: 635 units
Reason for Recall
Product may contain undeclared peanut, soy, and wheat.
Distribution
ME, NH, MA, CT
Type: Voluntary: Firm initiated
Recall Initiated: 2023-08-14
Company
York, ME
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 39 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Stonewall Kitchen, LLC 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 (Stonewall Kitchen, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Stonewall Kitchen, LLC have FDA actions?
Stonewall Kitchen, LLC 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-1476-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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