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Lower risk Food recall · FDA · Published February 17, 2021

Giant Eagle Pretzels with Undeclared Pecans: Recall Notice

Giant Eagle recalls Market District Gourmet Pretzel Gift Bags and Platters due to undeclared pecans in chocolate covered pretzels. Consumers should check product labels for PLU codes 45505 or 25206.

🇺🇸 FDA recall #F-0340-2021FoodGiant Eagle ›
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Recalling firmGiant Eagle267 Kappa Dr · Pittsburgh, PA 15238-2817
✎ GovInfoNow plain-language explainer

Giant Eagle is recalling two types of pretzel gift bags and platters because they contain undeclared pecans. This poses a risk for people with nut allergies who might consume the pretzels without knowing. Read more at govinfonow.com/recall/14849-giant-eagle-pretzels-with-undeclared-pecans-recall-notice.

Source Summary by GovInfoNow · govinfonow.com/recall/14849-giant-eagle-pretzels-with-undeclared-pecans-recall-notice · Updated October 4, 2026 · FDA enforcement record: FDA #F-0340-2021

Cite this page

“Giant Eagle Pretzels with Undeclared Pecans: Recall Notice.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14849-giant-eagle-pretzels-with-undeclared-pecans-recall-notice. Based on FDA recall #F-0340-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0340-2021%22&limit=1).

The FDA announced on Feb. 17, 2021, that Giant Eagle is recalling Market District Gourmet Pretzel Gift Bag and Platter due to undeclared pecans. Owners should stop consuming the product immediately.

How to tell if you have it

  • Brand: Giant Eagle
  • Product: Market District Gourmet Pretzel Gift Bag PLU 45505 Net Wt 9 oz
  • Product: Market District Gourmet Pretzel Platter PLU 25206 Net Wt 48 oz
  • Shelf life through 4/3/21
  • Distribution: OH and PA
  • Units affected: 192

The hazard

The products contain undeclared pecans, which pose a risk to individuals with nut allergies. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show Giant Eagle has issued four other recalls since Dec. 27, 2013. Similar recent recalls include the Carousel Candies Choceur Cookie Butter Holiday Bark Recall (Nov. 21, 2025) and the Albertsons Yellow Caramel Pecan Cake Recall (May 6, 2026).

How to tell if you have this one

Check for the product labels with PLU codes 45505 (9 oz gift bag) or 25206 (48 oz platter). The recall covers items sold up to April 3, 2021.

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

What to do — step by step

  1. Check Product Labels

    Look for PLU codes 45505 on the gift bag or 25206 on the platter to identify affected items.

Where it went and when

Where it was distributed

Distributed in Ohio and Pennsylvania.

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: not listedMDDelaware: 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: “Distributed in OH and PA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Ohio, Pennsylvania.

Recall timeline

FDA terminated this recall 13 months after the firm started it.

1. Firm started the recall: Feb 17, 202112. FDA classified it Class II: Mar 15, 202123. Published in FDA’s Enforcement Report: Mar 24, 202134. FDA terminated the recall: Mar 9, 2022420212022
  1. Firm started the recall
  2. FDA classified it Class II
  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-0340-2021 (February 17, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0340-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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