RecallHawk
Class I Recall

Imperial Fresh 4/5 LB CTN FRSH 1/4" DICED YLW ONIONS W/ZIP

Gills Onions, LLC

Summary

The FDA issued a Class I for Imperial Fresh 4/5 LB CTN FRSH 1/4" DICED YLW ONIONS W/ZIP by Gills Onions, LLC. Reason: Potential contamination with Salmonella Thompson.

Details

Source

Food Recall

External ID

F-0376-2024

Action Date

2023-11-15

Status

Terminated

Category

food

Product Description

Imperial Fresh 4/5 LB CTN FRSH 1/4" DICED YLW ONIONS W/ZIP

Lot/Code Info: SYSCO 4160768 (Product 6510142006SY); Finished product lots: 223YAC2B2R202 223YAM4B2R219 223YAM4B2R222 223YAS2A2R221 223YAS2B2R220 223YAS2B2R221 223YAS3A1P213 223YAS3A2R209 223YAS3A2R214 223YAS3A2R216 223YAS3B1P215 223YAS3B2R207 223YAS3B2R212 923Y072B2R202 923Y075B2R206 923Y077B2R208 923Y084B2R222

Quantity Affected: 69,420 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

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-0376-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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