Cbi Bg 2280/45025 recall
Recalled by Skidmore Sales & Distributing Co Inc · West Chester, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product contains undeclared soy lecithin.
Undeclared allergen: Soy
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
CBI BG 2280/45025, 50 lb. package, 1 poly bag in cardboard box, 1140496
Quantity: 24,500 lbs.
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
Kentucky
FDA's distribution note: Delivered to 1 customer located in Kentucky.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Skidmore Sales & Distributing Co Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 27, 2019
- In FDA report of
- Dec 18, 2019
- Terminated
- Feb 12, 2020
- FDA recall number
- F-0222-2020 · event 84387
- Official record
- FDA enforcement report search