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Class II: temporary or reversible health riskTerminated

Skidmore Sales & Distributing Cbi Bg 2280/45025 Recall

CBI BG 2280/45025, 50 lb

Skidmore Sales & Distributing Co Inc · West Chester, OH

Risk level
Class II
Reported by FDA
Dec 18, 2019
Recall ID
F-0222-2020
Check your lot numberHow we source this data

Summary

Skidmore Sales & Distributing recalled Cbi Bg 2280/45025 starting Nov 27, 2019. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0222-2020 on Dec 18, 2019. Reason: Product contains undeclared soy lecithin. Status: Terminated.

Why it was recalled

Product contains undeclared soy lecithin.

Product description

CBI BG 2280/45025, 50 lb. package, 1 poly bag in cardboard box, 1140496

Lot numbers, UPCs & expiration codes

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

Where it was sold

Delivered to 1 customer located in Kentucky.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0222-2020
Classification
Class II
Status
Terminated
Recall initiated
Nov 27, 2019
FDA report date
Dec 18, 2019
Quantity
24,500 lbs.
Recall type
Voluntary: Firm initiated
Recalling firm
Skidmore Sales & Distributing Co Inc

Original FDA data

Every field from FDA enforcement report F-0222-2020, exactly as published.

Show all FDA fields
City
West Chester
State
OH
Status
Terminated
Country
United States
Event ID
84387
Address
9889 Cincinnati Dayton Rd
Code information
LOT Mfg. Date Exp. Date L262 11/26/2012 11/26/2013; B223 2/22/2013 2/22/2014; C253 3/25/2013 3/25/2014; F053 6/5/2013 6/5/2014; G123 7/12/2013 7/12/2014; H293 8/29/2013 8/29/2014; K103 10/10/2013 10/10/2014; K303 10/30/2013 10/30/2014; L123 11/12/2013 11/12/2014; B064 2/6/2014 2/6/2015; C134 3/13/2014 3/13/2015; E054 5/5/2014 5/5/2015; F094 6/9/2014 6/9/2015; G074 7/7/2014 7/7/2015; H274 8/27/2014 8/27/2015; K094 10/9/2014 10/9/2015; L054 11/5/2014 11/5/2015; A055 1/5/2015 1/5/2016; A265 1/26/2015 1/26/2016; E225 5/22/2015 5/22/2016; F175 6/17/2015 6/17/2016; J285 9/28/2015 9/28/2016; K305 10/30/2015 10/30/2016; L245 11/24/2015 11/24/2016; D076 4/7/2016 4/7/2017; F026 6/2/2016 6/2/2017; H016 8/1/2016 8/1/2017; K206 10/20/2016 10/20/2017; C217 3/21/2017 3/21/2018; D247 4/24/2017 4/24/2018; G287 7/28/2017 7/28/2018; J147 9/14/2017 9/14/2018; K207 10/20/2017 10/20/2018; A228 1/22/2018 1/22/2019; B138 2/13/2018 2/13/2019; E038 5/3/2018 5/3/2019; F218 6/21/2018 6/21/2019; H068 8/6/2018 8/6/2019; K308 10/30/2018 10/30/2019; B279 2/27/2019 2/27/2020; D249 4/24/2019 4/24/2020; G099 7/9/2019 7/9/2020; H199 8/16/2019 8/16/2020; K099 10/4/2019 10/4/2020; L229 11/22/2019 11/22/2020.
Postal code
45069-3825
Report date
Dec 18, 2019
Product type
Food
Recall number
F-0222-2020
Classification
Class II
Recalling firm
Skidmore Sales & Distributing Co Inc
Product quantity
24,500 lbs.
Termination date
Feb 12, 2020
Reason for recall
Product contains undeclared soy lecithin.
Voluntary / mandated
Voluntary: Firm initiated
Product description
CBI BG 2280/45025, 50 lb. package, 1 poly bag in cardboard box, 1140496
Distribution pattern
Delivered to 1 customer located in Kentucky.
Recall initiation date
Nov 27, 2019
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Dec 9, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0222-2020, published Dec 18, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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