Summary
The FDA issued a Class I for Ready Set Serve 4/5 LB CTN FRESH 1/4" DICED YLW ONIONS W/ZIP by Gills Onions, LLC. Reason: Potential contamination with Salmonella Thompson.
Details
Source
Food Recall
External ID
F-0397-2024
Action Date
2023-11-15
Status
Terminated
Category
food
Product Description
Ready Set Serve 4/5 LB CTN FRESH 1/4" DICED YLW ONIONS W/ZIP
Lot/Code Info: Product 6510142007MK; Finished product lots: 223YAS1B2R216 223YAS1B2R221 223YAS2B2R215 223YAS3A2R208 223YAS3B2R212 223YAS3B2R214 223YAS3B2R215 923Y071B2R202 923Y074A2R206 923Y077B2R208 923Y081B2R221 923Y085B2R222
Quantity Affected: 23,300 lb
Reason for Recall
Potential contamination with Salmonella Thompson
Distribution
Distributors in Canada AB, BC, NB, NS, ON; and the United States AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NM, NV, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA and WI.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-10-23
Company
Oxnard, CA
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 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Gills Onions, LLC has 73 FDA actions in our database, including 73 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 (Gills Onions, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Gills Onions, LLC have FDA actions?
Gills Onions, LLC has 73 FDA actions in our database, including 73 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0397-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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