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Lower risk Food recall · FDA · Published October 19, 2017

Giant Eagle Breaded Shrimp Recall: Undeclared Egg Allergen Risk

Giant Eagle voluntarily recalls Breaded Shrimp (PLU #86815) sold through Oct 19, 2017 due to undeclared egg allergen. Consumers should avoid products with lot codes up to best by Oct 24, 2017.

🇺🇸 FDA recall #F-0334-2018FoodGiant Eagle ›
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Recalling firmGiant Eagle, Inc.101 Kappa Dr · Pittsburgh, PA 15238-2809
✎ GovInfoNow plain-language explainer

What happened, in plain English

Giant Eagle is recalling Breaded Shrimp products that may contain an undeclared egg allergen. This poses a risk for people with egg allergies who could experience an allergic reaction. The recall affects products sold in their grab-and-go sections through October 19, 2017. Read more at govinfonow.com/recall/20276-giant-eagle-breaded-shrimp-recall-undeclared-egg-allergen-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/20276-giant-eagle-breaded-shrimp-recall-undeclared-egg-allergen-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0334-2018

Cite this page

“Giant Eagle Breaded Shrimp Recall: Undeclared Egg Allergen Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20276-giant-eagle-breaded-shrimp-recall-undeclared-egg-allergen-risk. Based on FDA recall #F-0334-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0334-2018%22&limit=1).

Why it’s dangerous

The product contains an undeclared egg allergen, meaning it may be unsafe for individuals with egg allergies. This could cause an allergic reaction in sensitive consumers. The recall specifically targets products sold through October 19, 2017.

Who’s affected

People with egg allergies are at risk of an allergic reaction from this product. The recall applies to Giant Eagle Breaded Shrimp sold in grab-and-go sections through October 19, 2017.

How to tell if you have this one

Check for the PLU number 86815 on the product packaging. Products were sold in Giant Eagle and Market District supermarkets' grab-and-go refrigerated sections through October 19, 2017. The sell-by date is up to and including October 24, 2017.

  • Brand
    Giant Eagle
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the PLU number 86815 on the product packaging to confirm it's part of the recall.

Where it went and when

Where it was distributed

Distributed in 3 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: not listedWVVirginia: 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” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maryland, Ohio, Pennsylvania.

Recall timeline

FDA terminated this recall 12 months after the firm started it.

1. Firm started the recall: Oct 19, 201712. FDA classified it Class I: Nov 17, 201723. Published in FDA’s Enforcement Report: Nov 22, 201734. FDA terminated the recall: Oct 26, 2018420172018
  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-0334-2018 (October 19, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0334-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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