raw, yellow onions (whole peeled), intended for food service, packaged into plastic bags (5-lbs)
Summary
The FDA issued a Class I for raw, yellow onions (whole peeled), intended for food service, packaged into plas by Taylor Farms Colorado, Inc.. Reason: Potential contamination of E. coli O157:H7.
Details
Source
Food Recall
External ID
F-0134-2025
Action Date
2024-11-20
Status
Terminated
Category
food
Product Description
raw, yellow onions (whole peeled), intended for food service, packaged into plastic bags (5-lbs)
Lot/Code Info: Taylor Farm Colorado lot codes, 'TFCO' Julian dates 278, 281-285, 288-292, and 295 277-279, 281-286, 288-292; 'USE THRU' from '18 OCT 2024' to '3 NOV 2024'
Quantity Affected: 615 cases
Reason for Recall
Potential contamination of E. coli O157:H7
Distribution
To food service facilities in CO, KS, MO, NE, NM, UT
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-22
Company
Colorado Springs, CO
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 38 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Taylor Farms Colorado, Inc. has 4 FDA actions in our database, including 4 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 (Taylor Farms Colorado, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Taylor Farms Colorado, Inc. have FDA actions?
Taylor Farms Colorado, Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0134-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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