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Lower risk Food recall · FDA · Published November 27, 2019

Skidmore Recalls Soy Lecithin Product Due to Undeclared Ingredient

Skidmore recalls 50-lb soy lecithin packages with undeclared soy lecithin. Consumers should check product labels for lot numbers and contact Skidmore for details.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #F-0222-2020FoodSkidmore ›
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Contact the company

Recalling firmSkidmore Sales & Distributing Co Inc9889 Cincinnati Dayton Rd · West Chester, OH 45069-3825
✎ GovInfoNow plain-language explainer

Skidmore is recalling 50-pound soy lecithin packages that contain undeclared soy lecithin. This issue does not pose a health risk but is a regulatory compliance problem. Read more at govinfonow.com/recall/16210-skidmore-recalls-soy-lecithin-product-due-to-undeclared-ingredient.

Source Summary by GovInfoNow · govinfonow.com/recall/16210-skidmore-recalls-soy-lecithin-product-due-to-undeclared-ingredient · Updated October 5, 2026 · FDA enforcement record: FDA #F-0222-2020

Cite this page

“Skidmore Recalls Soy Lecithin Product Due to Undeclared Ingredient.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16210-skidmore-recalls-soy-lecithin-product-due-to-undeclared-ingredient. Based on FDA recall #F-0222-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0222-2020%22&limit=1).

The Food and Drug Administration announced on Nov. 27, 2019, that Skidmore Sales & Distributing Co Inc voluntarily recalled CBI BG 2280/45025 due to undeclared soy lecithin. The agency issued recall number F-0222-2020 for the product.

How to tell if you have it

  • Brand: Skidmore
  • Product: CBI BG 2280/45025
  • Package: 50 lb. package, 1 poly bag in cardboard box
  • UPC/Lot: 1140496
  • Lot codes: L262, B223, C253, F053, G123, H293, K103, K303, L123, B064, C134, E054, F094, G074, H274, K094, L054, A055, A265, E225, F175, J285, K305, L245, D076, F026, H016, K206, C217, D247, G287, J147, K207, A228, B138, E038, F218, H068, K308, B279, D249, G099, H199, K099, L229
  • Units affected: 24,500 lbs.

The hazard

The product contains undeclared soy lecithin. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include Prospector Popcorn Recall: Undeclared Soy Hazard (2026-04-28), Zarlengo Gelato Recall: Soy Lecithin Missing from Contains Statement (2026-03-26), and BEF Foods Park St. Deli Macaroni & Cheese Recall: Undeclared Soy Lecithin Allergen (2026-03-23).

How to tell if you have this one

Check for the product name 'CBI BG 2280/45025', 50 lb. package in a poly bag inside a cardboard box. Look for lot numbers listed in the recall notice, such as L262, B223, etc.

  • Brand
    Skidmore
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot number on the product label, which is listed in the recall notice (e.g., L262, B223).

  2. Contact Skidmore

    Reach out to Skidmore Sales & Distributing Co Inc for further assistance or to confirm if your product is affected.

Where it went and when

Where it was distributed

Distributed in Kentucky.

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: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: yesKYWest 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: “Delivered to 1 customer located in Kentucky.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Kentucky.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Nov 27, 201912. FDA classified it Class II: Dec 9, 201923. Published in FDA’s Enforcement Report: Dec 18, 201934. FDA terminated the recall: Feb 12, 2020420192020
  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-0222-2020 (November 27, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0222-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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