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Stop using now Food recall · FDA · Published October 14, 2018

Fred Meyer Recalls Angel Food Cake Bars for Undeclared Milk and Soy

Fred Meyer Inc. recalls Angel Food Cake Bars due to undeclared milk and soy allergens. Check your black tray packaging with UPC 111110-02100.

🇺🇸 FDA recall #F-0371-2019FoodFred Meyer ›
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Recalling firmFred Meyer Inc.16253 SE 122nd Ave · Clackamas, OR 97015-9136
✎ GovInfoNow plain-language explainer

What happened, in plain English

Fred Meyer Inc. is recalling 'Angel Food Cake Bar' products because they were mislabeled. The packages labeled as cake bars actually contain cornbread, which contains undeclared milk and soy allergens. This poses a risk to individuals with allergies to these ingredients. Read more at govinfonow.com/recall/18333-fred-meyer-recalls-angel-food-cake-bars-for-undeclared-milk.

Source Summary by GovInfoNow · govinfonow.com/recall/18333-fred-meyer-recalls-angel-food-cake-bars-for-undeclared-milk · Updated October 11, 2026 · FDA enforcement record: FDA #F-0371-2019

Cite this page

“Fred Meyer Recalls Angel Food Cake Bars for Undeclared Milk and Soy.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/18333-fred-meyer-recalls-angel-food-cake-bars-for-undeclared-milk. Based on FDA recall #F-0371-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0371-2019%22&limit=1).

Why it’s dangerous

The product contains undeclared milk and soy because it is actually cornbread, not cake. Consuming these allergens can cause serious allergic reactions in sensitive individuals.

Who’s affected

Consumers who purchased the mislabeled 'Angel Food Cake Bar' products distributed in Oregon and Washington are affected. Individuals with milk or soy allergies are at the highest risk of an allergic reaction.

How to tell if you have this one

Look for 'Angel Food Cake Bar' packaged in black plastic trays with a clear plastic dome lid. The label should show a net weight of 12 oz and the UPC 111110-02100. The label also states it is distributed by Inter-American Products, Inc. in Cincinnati, OH.

  • Brand
    Fred Meyer
  • Product
    Product 8x8 " individually packaged in black plastic trays with clear plastic dome lid is cornbread and it was
  • Category
    Food

Where it went and when

Where it was distributed

Distributed in Oregon and Washington.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew 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 OR, and WA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Oregon, Washington.

Recall timeline

FDA terminated this recall 31 days after the firm started it.

1. Firm started the recall: Oct 14, 201812. FDA classified it Class I: Nov 6, 201823. Published in FDA’s Enforcement Report: Nov 14, 201834. FDA terminated the recall: Nov 14, 201842018
  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-0371-2019 (October 14, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0371-2019 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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