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

FDA Recall #F-0222-2020 — Class II — November 27, 2019

Recall Summary

Recall NumberF-0222-2020
Date InitiatedNovember 27, 2019
ClassificationClass II
StatusTerminated
TypeVoluntary: Firm initiated
Product TypeFood

Recalling Firm

FirmSkidmore Sales & Distributing Co Inc
LocationWest Chester, OH

Product Description

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

Reason for Recall

Product contains undeclared soy lecithin.

Classification

Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

Distribution Pattern

Delivered to 1 customer located in Kentucky.

Product Quantity

24,500 lbs.

Product Codes / Lot Numbers

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.

What Should You Do?

Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.

Frequently Asked Questions

Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.

If you have a food allergy and consumed the recalled product, monitor yourself closely for allergic reaction symptoms — including hives, swelling, difficulty breathing, nausea, vomiting, or anaphylaxis. If you experience any symptoms, seek medical attention immediately. For anaphylaxis (severe allergic reaction with difficulty breathing, rapid heartbeat, or loss of consciousness), call 911 and use an epinephrine auto-injector (EpiPen) if available. Stop consuming the product and check all products from the same manufacturer for similar labeling issues, as undeclared allergens sometimes affect multiple products from the same production facility.

Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.

The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.