Fry Pie Factory LLC Pepperoni Rolls Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Fry Pie Factory LLC is recalling 850 units of Pepperoni Rolls due to undeclared milk and refrigeration process deviation.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 6, 2026 and geographically references Ohio and West Virginia. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
What Happened
Fry Pie Factory LLC initiated a voluntary recall of Pepperoni Rolls because of an undeclared milk allergen and a process deviation where the product was not held under refrigeration as required.
Which Products Are Affected
The recall covers Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic bag with UPC 601959803041. A total of 850 individual units are affected, with sell by dates 061226 through 062126. The products were distributed in OH and WV.
What You Should Do
Consumers should not consume the recalled products. Contact information for returns or refunds was not provided in the recall notice.
Why This Matters
The recall addresses potential allergen exposure and food safety risks from improper refrigeration in a Class II recall affecting 850 units in two states.
Source
FDA recall number H-1136-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (873 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 6, 2026.
Frequently Asked Questions
Common questions about this FDA recall.