Item Number PACK/SZ BRAND DESCRIPTION Lot Codes 082076 4/5 LBS IMPERIALFRESH PROC ONION YELLOW JULIENNE 3/8 All lot code
Summary
The FDA issued a Class I for Item Number PACK/SZ BRAND DESCRIPTION Lot Codes 082076 4/5 LBS IMPERIALFRESH PRO by FreshPoint Denver, Incorporated. Reason: Potentially contaminated with E. coli O157:H7..
Details
Source
Food Recall
External ID
F-0137-2025
Action Date
2024-11-20
Status
Terminated
Category
food
Product Description
Item Number PACK/SZ BRAND DESCRIPTION Lot Codes 082076 4/5 LBS IMPERIALFRESH PROC ONION YELLOW JULIENNE 3/8 All lot codes; 170992 4/5 LB IMPERIALFRESH PROC ONION YELLOW DICED 3/8 All lot codes; 258147 4/5LBS IMPERIALFRESH PROC ONION YELLOW JULIENNE 1/4 All lot codes; 259369 1 / 5 LB IMPERIALFRESH PROC ONION YELLOW JULIENNE 1/4 All lot codes; 710372 4 / 5 LB IMPERIALFRESH PROC ONION YELLOW DICED 1/4 All lot codes; 728725 1 / 5 LB IMPERIALFRESH PROC ONION YELLOW DICED 1/4 All lot codes; 106360 1/5 LB IMPERIALFRESH PROC ONION YELLOW DICED 3/8 All lot codes; 235482 2/5 LB IMPERIALFRESH PROC ONION YELLOW DICED All lot codes; 329525 2/5 LB IMPERIALFRESH PROC ONION YELLOW DICED All lot codes; 871953 4/5 LB IMPERIALFRESH PROC ONION YELLOW DICE All lot codes. Packed in Cardboard cases with trays
Lot/Code Info: All lot codes of the recalled products listed above produced between 10/8/2024 and 10/22/2024
Quantity Affected: 67 cases (5lbs per case)
Reason for Recall
Potentially contaminated with E. coli O157:H7.
Distribution
Colorado
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-22
Company
Denver, 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.
FreshPoint Denver, Incorporated has 2 FDA actions in our database, including 2 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 (FreshPoint Denver, Incorporated) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does FreshPoint Denver, Incorporated have FDA actions?
FreshPoint Denver, Incorporated has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0137-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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