Lower riskFood recall · FDA · Published March 22, 2015
Giant Eagle Little Italy Panini Cold has undeclared egg - recall
Giant Eagle recalls Little Italy Panini Cold products with undeclared egg. These items contain wheat, milk, and fish. Consumers should check product labels for PLU numbers 97525 (cold) or 7369 (hot).
“Giant Eagle Little Italy Panini Cold has undeclared egg - recall.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/27218-giant-eagle-little-italy-panini-cold-has-undeclared-egg-recall. Based on FDA recall #F-1931-2015 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1931-2015%22&limit=1).
Giant Eagle, Inc. recalled Giant Eagle Little Italy Panini Cold and Hot products due to undeclared egg allergens, the FDA said on March 22, 2015. The recall covers items sold in Pennsylvania with sell-by dates through March 24, 2015.
How to tell if you have it
Brand: Giant Eagle
Product: Little Italy Panini Cold and Hot
PLU #97525 (Cold), PLU #7369 (Hot)
Sell-by dates up to and including 3/24/2015 (Cold) and 3/22/2015 (Hot)
Distribution: PA
Units affected: 66
The hazard
The Little Italy Panini products contain undeclared egg, posing an allergy risk to consumers. The FDA classified the recall as Class I.
Context
GovInfoNow's records show Giant Eagle, Inc. has had 29 other recalls since December 3, 2014. Recent similar recalls include a March 29, 2022 undeclared milk allergen risk for Happy Face Cookie and an October 2, 2025 potential listeria contamination for Smoked Mozzarella Penne Salad. Other recent recalls of similar products include a July 29, 2026 undeclared egg allergen risk for Kerry KC Everyday Mac & Cheese, a February 26, 2026 undeclared egg hazard for House of Flavors Vanilla Ice Cream, and a September 8, 2026 undeclared egg allergen in cheese from Fromagerie Coop de Mean Cabricharme.
How to tell if you have this one
Check for PLU number 97525 on cold paninis or 7369 on hot paninis. Products sold up to March 24, 2015 are affected.
Brand
Giant Eagle
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for PLU numbers 97525 (cold) or 7369 (hot) on the product packaging.
Where it went and when
Where it was distributed
Distributed in Pennsylvania.
Listed by the agency
Not listed
FDA distribution: “PA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Pennsylvania.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-1931-2015 (March 22, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1931-2015 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.