FreshPoint Denver, Incorporated Recall: Potentially contaminated with E. coli O157:H7.

United States

TerminatedClass I

Company: FreshPoint Denver, Incorporated
Product: Item Number PACK/SZ BRAND DESCRIPTION Lot Codes 082076 4/5 L…
Recall date: October 22, 2024
Terminated: February 6, 2026
Source: FDA

Reason for recall

Potentially contaminated with E. coli O157:H7.

October 22, 2024 - Recall initiated
November 20, 2024 - Reported by source
February 6, 2026 - Recall terminated

Recalled products
Product description	UPC	Quantity	Lot / code information
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	Not published in this source record	67 cases (5lbs per case)	All lot codes of the recalled products listed above produced between 10/8/2024 and 10/22/2024

Distribution

Colorado

Official source record

Agency: FDA
Dataset: FDA Food Enforcement (Recalls)
Recall number: F-0137-2025
Event ID: 95622
Status: Terminated
Classification: Class I
Company: FreshPoint Denver, Incorporated
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
Quantity: 67 cases (5lbs per case)
Reason: Potentially contaminated with E. coli O157:H7.
Recall initiation date: October 22, 2024
Report date: November 20, 2024
Classification date: Not published in this source record
Termination date: February 6, 2026
Distribution pattern: Colorado
UPC, lot, and code information: All lot codes of the recalled products listed above produced between 10/8/2024 and 10/22/2024
Voluntary or mandated: Voluntary: Firm initiated
Initial notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated: Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date: July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 95622 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

FreshPoint Denver, Incorporated

Product: 154784 1 / 5LB IMPERIALFRESH PROC FAJITA GRN PEPRED PEP W Al…
Published: November 20, 2024
Distribution: Colorado

View recall →

Responsible company: FreshPoint Denver, Incorporated

Other recalls from FreshPoint Denver, Incorporated

FDA Recall United States Terminated Historical recordClass I

FreshPoint Denver, Incorporated

Product: 154784 1 / 5LB IMPERIALFRESH PROC FAJITA GRN PEPRED PEP W Al…
Published: November 20, 2024
Distribution: Colorado

View recall →

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

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