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Use caution Food recall · FDA · Published April 28, 2021

Croissant Etc Recalls Frozen Croissant Crusts Due to Undeclared Soy

Croissant Etc Corp recalls frozen 6-inch round croissant crusts because they contain undeclared soy lecithin, posing a risk to those with soy allergies.

🇺🇸 FDA recall #F-0629-2021FoodCroissant Etc ›
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Recalling firmCroissant Etc Corp7195 S 1st St · Oak Creek, WI 53154-2001
✎ GovInfoNow plain-language explainer

What happened, in plain English

Croissant Etc Corp is recalling 20 cases of its 6-inch Round Croissant Crust (100 Count Bulk) distributed in Minnesota. The product contains undeclared soy lecithin, which can cause allergic reactions in sensitive individuals. The recall was issued on April 28, 2021. Read more at govinfonow.com/recall/14576-croissant-etc-recalls-frozen-croissant-crusts-due-to-undeclared-soy.

Source Summary by GovInfoNow · govinfonow.com/recall/14576-croissant-etc-recalls-frozen-croissant-crusts-due-to-undeclared-soy · Updated October 10, 2026 · FDA enforcement record: FDA #F-0629-2021

Cite this page

“Croissant Etc Recalls Frozen Croissant Crusts Due to Undeclared Soy.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/14576-croissant-etc-recalls-frozen-croissant-crusts-due-to-undeclared-soy. Based on FDA recall #F-0629-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0629-2021%22&limit=1).

Why it’s dangerous

The undeclared soy lecithin poses a health risk to people with soy allergies because the ingredient is not listed on the label. Ingesting the product could trigger an allergic response in susceptible individuals.

Who’s affected

Consumers in Minnesota who purchased the recalled frozen croissant crusts are affected. Individuals with soy allergies or sensitivities are at risk of an allergic reaction if they consume the product.

How to tell if you have this one

Check for 6-inch round croissant crusts sold in 100-count bulk packages with a net weight of 6.25 lbs. Look for the manufacturer name 'Croissant Etc Corp' from Greendale, WI, and check if the Mfg. Date is 210412 or the Use by date is July 12, 2021.

  • Brand
    Croissant Etc
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled croissant crusts if you have a soy allergy or are unsure about the ingredients.

  2. Check your purchase details

    Verify that your product matches the 6-inch round, 100-count bulk package with Mfg. Date 210412 or Use by July 12, 2021.

  3. Contact the manufacturer

    Reach out to Croissant Etc Corp in Greendale, WI for further information on the recall process.

Where it went and when

Where it was distributed

Distributed in Minnesota.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: 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: 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: “MN” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Minnesota.

Recall timeline

FDA terminated this recall 48 days after the firm started it.

1. Firm started the recall: Apr 28, 202112. FDA classified it Class II: May 25, 202123. Published in FDA’s Enforcement Report: Jun 2, 202134. FDA terminated the recall: Jun 15, 202142021
  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-0629-2021 (April 28, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0629-2021 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 10, 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