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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Packaged & Processed

CBI BG 2280/45025 Food Product Recalled for Undeclared Soy Lecithin

Agency Publication Date: December 9, 2019
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Summary

Skidmore Sales & Distributing Co Inc has recalled approximately 24,500 pounds of CBI BG 2280/45025 because it contains soy lecithin, an allergen that was not declared on the product label. The recall affects 50 lb. packages consisting of a poly bag inside a cardboard box. This product was delivered to a single customer in Kentucky and includes numerous manufacturing lots produced between 2012 and 2019.

Risk

People who have an allergy or severe sensitivity to soy run the risk of a serious or life-threatening allergic reaction if they consume this product.

What You Should Do

  1. Check your inventory for 50 lb. packages of CBI BG 2280/45025 (item code 1140496) featuring a poly bag inside a cardboard box.
  2. Identify affected products by checking the lot number, manufacturing date, and expiration date printed on the packaging. See the Affected Products section below for the full list of affected codes.
  3. Return the product to the place of purchase for a full refund, throw it away, or contact Skidmore Sales & Distributing Co Inc for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: CBI BG 2280/45025 (50 lb. package)
Item Code:
1140496
Lot Numbers:
L262 (Mfg. 11/26/2012, Exp. 11/26/2013)
B223 (Mfg. 2/22/2013, Exp. 2/22/2014)
C253 (Mfg. 3/25/2013, Exp. 3/25/2014)
F053 (Mfg. 6/5/2013, Exp. 6/5/2014)
G123 (Mfg. 7/12/2013, Exp. 7/12/2014)
H293 (Mfg. 8/29/2013, Exp. 8/29/2014)
K103 (Mfg. 10/10/2013, Exp. 10/10/2014)
K303 (Mfg. 10/30/2013, Exp. 10/30/2014)
L123 (Mfg. 11/12/2013, Exp. 11/12/2014)
B064 (Mfg. 2/6/2014, Exp. 2/6/2015)
C134 (Mfg. 3/13/2014, Exp. 3/13/2015)
E054 (Mfg. 5/5/2014, Exp. 5/5/2015)
F094 (Mfg. 6/9/2014, Exp. 6/9/2015)
G074 (Mfg. 7/7/2014, Exp. 7/7/2015)
H274 (Mfg. 8/27/2014, Exp. 8/27/2015)
K094 (Mfg. 10/9/2014, Exp. 10/9/2015)
L054 (Mfg. 11/5/2014, Exp. 11/5/2015)
A055 (Mfg. 1/5/2015, Exp. 1/5/2016)
A265 (Mfg. 1/26/2015, Exp. 1/26/2016)
E225 (Mfg. 5/22/2015, Exp. 5/22/2016)
F175 (Mfg. 6/17/2015, Exp. 6/17/2016)
J285 (Mfg. 9/28/2015, Exp. 9/28/2016)
K305 (Mfg. 10/30/2015, Exp. 10/30/2016)
L245 (Mfg. 11/24/2015, Exp. 11/24/2016)
D076 (Mfg. 4/7/2016, Exp. 4/7/2017)
F026 (Mfg. 6/2/2016, Exp. 6/2/2017)
H016 (Mfg. 8/1/2016, Exp. 8/1/2017)
K206 (Mfg. 10/20/2016, Exp. 10/20/2017)
C217 (Mfg. 3/21/2017, Exp. 3/21/2018)
D247 (Mfg. 4/24/2017, Exp. 4/24/2018)
G287 (Mfg. 7/28/2017, Exp. 7/28/2018)
J147 (Mfg. 9/14/2017, Exp. 9/14/2018)
K207 (Mfg. 10/20/2017, Exp. 10/20/2018)
A228 (Mfg. 1/22/2018, Exp. 1/22/2019)
B138 (Mfg. 2/13/2018, Exp. 2/13/2019)
E038 (Mfg. 5/3/2018, Exp. 5/3/2019)
F218 (Mfg. 6/21/2018, Exp. 6/21/2019)
H068 (Mfg. 8/6/2018, Exp. 8/6/2019)
K308 (Mfg. 10/30/2018, Exp. 10/30/2019)
B279 (Mfg. 2/27/2019, Exp. 2/27/2020)
D249 (Mfg. 4/24/2019, Exp. 4/24/2020)
G099 (Mfg. 7/9/2019, Exp. 7/9/2020)
H199 (Mfg. 8/16/2019, Exp. 8/16/2020)
K099 (Mfg. 10/4/2019, Exp. 10/4/2020)
L229 (Mfg. 11/22/2019, Exp. 11/22/2020)

1 poly bag in cardboard box.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84387
Status: Resolved
Manufacturer: Skidmore Sales & Distributing Co Inc
Manufactured In: United States
Units Affected: 24,500 lbs.
Distributed To: Kentucky

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.