Whole raw WHITE onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb.,
Summary
The FDA issued a Class I for Whole raw WHITE onions are imported from Chihuahua of MEXICO. Products are pac by ProSource Produce LLC. Reason: Salmonella Oranienburg..
Details
Source
Food Recall
External ID
F-0113-2022
Action Date
2021-11-10
Status
Terminated
Category
food
Product Description
Whole raw WHITE onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3 lb., and 2 lb. mesh sacks and in 50 lb., 40 lb., 25 lb., 10 lb., and 5 lb. cartons. Products are distributed and/or sold under the brands Big Bull, Markon First Crop, Markon Essentials, Peak Fresh Produce, Rio Blue, Rio Valley, ProSource, Sierra Madre, and Sysco Imperial Fresh.
Lot/Code Info: Lot Codes for all WHITE onions: 221 222 230 306 1120 IGV191OWSB191 IGV221OWSB198 IGV31OWSB215 RMKLC191OWSB177 TYJ4M61OWSB182 TYJ4M61OWSB183 TYJ4M61OWSB186 VBAOWSB VBDPKWSB VBFGWSB VBJGWNB VBJRPWSB VBPNWSB VBTLWSB
Quantity Affected: 2,539,656 lbs.
Reason for Recall
Salmonella Oranienburg.
Distribution
Distributed in AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, VA, and WI, as well as Ontario and Quebec, Canada.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-20
Company
Hailey, ID
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.
ProSource Produce LLC has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (ProSource Produce LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does ProSource Produce LLC have FDA actions?
ProSource Produce LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0113-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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