Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic bag, UPC 601959803041
Summary
The FDA issued a Class II for Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic b by Fry Pie Factory LLC. Reason: Undeclared allergen (milk) and process deviation (product not held under refrigeration as required).
Details
Source
Food Recall
External ID
H-1136-2026
Action Date
2026-07-08
Status
Completed
Category
food
Product Description
Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic bag, UPC 601959803041
Lot/Code Info: Sell by dates 061226 through 062126
Quantity Affected: 850 individual units
Reason for Recall
Undeclared allergen (milk) and process deviation (product not held under refrigeration as required)
Distribution
OH, WV
Type: Voluntary: Firm initiated
Recall Initiated: 2026-06-10
Company
Lancaster, OH
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 54 food recalls issued in the same week, part of 101 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Fry Pie Factory LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Fry Pie Factory LLC have FDA actions?
This is the only FDA action we have on record for Fry Pie Factory LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1136-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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