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Use caution Food recall · FDA · Published March 31, 2015

Giant Eagle recalls GetGo Italian subs due to undeclared egg allergen

Giant Eagle voluntarily recalls GetGo 7-inch Italian subs sold up to April 2, 2015, because they contain undeclared egg allergen. Consumers should avoid these products to prevent allergic reactions.

🇺🇸 FDA recall #F-2024-2015FoodGiant Eagle ›
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Recalling firmGiant Eagle, Inc.101 Kappa Dr · Pittsburgh, PA 15238-2809
✎ GovInfoNow plain-language explainer

Giant Eagle is recalling GetGo 7-inch Italian subs sold up to April 2, 2015, because they contain an undeclared egg allergen. This poses a risk for people with egg allergies who might experience allergic reactions if they consume the product. Read more at govinfonow.com/recall/27174-giant-eagle-recalls-getgo-italian-subs-due-to-undeclared-egg.

Source Summary by GovInfoNow · govinfonow.com/recall/27174-giant-eagle-recalls-getgo-italian-subs-due-to-undeclared-egg · Updated August 18, 2026 · FDA enforcement record: FDA #F-2024-2015

Cite this page

“Giant Eagle recalls GetGo Italian subs due to undeclared egg allergen.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/27174-giant-eagle-recalls-getgo-italian-subs-due-to-undeclared-egg. Based on FDA recall #F-2024-2015 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2024-2015%22&limit=1).

The FDA announced on March 31, 2015, that Giant Eagle, Inc. voluntarily recalled GetGo GNG 7 Inch Italian Subs due to undeclared egg allergens. The recall affects products sold in Maryland, Ohio, Pennsylvania, and West Virginia.

How to tell if you have it

  • Brand: GetGo
  • Product: GNG 7 Inch Italian Sub
  • Sell By Date: (up to and including) 04/02/15
  • Net Weight: 6.0 Oz.
  • Contains: Soy, Milk, Wheat
  • UPC: 25567 20399

The hazard

The recall is due to the presence of undeclared egg allergens in the GetGo GNG 7 Inch Italian Subs. The FDA classified this as a Class I recall, indicating a high risk of adverse health consequences.

Context

GovInfoNow's records show Giant Eagle, Inc. has had 29 other recalls on record since December 3, 2014. Recent brand recalls include a potential listeria contamination issue reported on October 2, 2025, and foreign glass risks noted on April 12, 2025. Other recent recalls of similar products include Kerry KC Everyday Mac & Cheese (July 29, 2026), Fromagerie Coop de Mean Cabricharme (September 8, 2026), and E & S Grocery Taro Cakes (January 30, 2026).

How to tell if you have this one

Look for GetGo 7-inch Italian subs with a sell-by date up to April 2, 2015, and UPC 25567 20399. The product is wrapped in plastic and contains soy, milk, and wheat.

  • Brand
    Giant Eagle
  • Product
    GetGo GNG 7 Inch Italian Sub Sell By: (up to and including) 04/02/15 Net Wt: 6.0 Oz. Contains: Soy, Milk, Wheat UPC
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    MD OH PA WV
Recall numberProduct, codes & lotsQuantity
F-2024-2015GetGo GNG 7 Inch Italian Sub Sell By: (up to and including) 04/02/15 Net Wt: 6.0 Oz. Contains: Soy, Milk, Wheat UPC: 25567 20399 GetGo from Giant Eagle Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238 Sandwich is wrapped in plastic.; Sell By: (up to and including) 04/02/15 UPC: 25567 203994671 units
F-2025-2015GetGo GNG 7 Inch Turkey N Swiss Sell By: (up to and including) 04/02/15 Net Wt: 6.0 Oz. Contains: Milk, Soy, Wheat; UPC: 65567 20399 GetGo from Giant Eagle Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238 Sandwich is wrapped in plastic.; Sell By: (up to and including) 04/02/15 UPC: 65567 203992332 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the sell-by date up to April 2, 2015, and UPC 25567 20399 on the product.

Where it went and when

Where it was distributed

Distributed in 4 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: yesWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “MD OH PA WV” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maryland, Ohio, Pennsylvania, West Virginia.

Recall timeline

FDA terminated this recall 57 days after the firm started it.

1. Firm started the recall: Mar 31, 201512. FDA classified it Class I: Apr 22, 201523. Published in FDA’s Enforcement Report: Apr 29, 201534. FDA terminated the recall: May 27, 201542015
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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-2024-2015 (March 31, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2024-2015 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA