Class IITerminated in FDA datasetNov 27, 2019

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

Recalling firm: Skidmore Sales & Distributing Co Inc

Why it was recalled

Product contains undeclared soy lecithin.

Check the codes ↓

The exact product

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

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA 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.

Recall details

Recall number
F-0222-2020
Event ID
84387
FDA status
Terminated
Initiated
Nov 27, 2019
Reported
Dec 18, 2019
Classified
Dec 9, 2019
Terminated
Feb 12, 2020
Quantity
24,500 lbs.
Location
West Chester, OH, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Delivered to 1 customer located in Kentucky.

FDA source record · F-0222-2020

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.