FDA recall, , Moderate risk
Fry Pie Factory Pepperoni Rolls
Pepperoni Rolls contain undeclared milk and were not refrigerated as required, posing a risk of allergic reaction or food-borne illness.
Recall ended Aug 24, 2026. Still check yours.
What happened
Fry Pie Factory LLC of Lancaster, Ohio, recalled its Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic bag, due to misbranding involving undeclared milk, a known allergen, and a process deviation related to refrigeration. The company began the recall on June 10, 2026, and announced it on June 12, 2026. The recall involved 850 individual units distributed in Ohio and West Virginia.
The product was added to the FDA's Enforcement Report on July 1, 2026, and in the FDA's weekly enforcement report on July 8, 2026. The recall was prompted by the undeclared milk and the process deviation.
What to do
If a code on your package is listed below:
- Anyone experiencing signs of an allergic reaction or food-borne illness should contact a health care provider immediately.
- Discard the Pepperoni Rolls or return them to Fry Pie Factory for a full refund.
- Customers with questions may contact Mark Thompson at 405-990-4657.
Is yours affected?
Affected if its UPC matches.
A UPC is the number printed under a barcode.
- UPC
- 601959803041
From the FDA notice
5 oz (141g), individually packaged in a clear plastic bag, UPC 601959803041
Recall details
- Company began the recall
- Sold in
- Company
- Fry Pie Factory LLCLancaster, Ohio
- Hazard
- Undeclared milk
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99275
- Recall number
- H-1136-2026
- Quantity recalled
- 850 individual units
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Announced by the company
Listed on Recall Canary
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Recall ended
Summary updated



