CLASS I Food recall · Reported 20 Nov 2024 · FDA Enforcement Report

154784 1 / Imperialfresh Proc Fajita Grn Pepred Pep W All lot codes recalled

FreshPoint Denver, Incorporated is recalling 154784 1 / Imperialfresh Proc Fajita Grn Pepred Pep W All lot codes, distributed in Colorado. The recall was initiated on 22 Oct 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll lot codes of the recalled products listed above produced between 10/8/2024 and 10/22/2024
Quantity recalled7 cases (5lbs ea case)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0138-2025
FDA event ID
95622
Recalling firm
FreshPoint Denver, Incorporated, Denver, CO
Classification
Class I
Status
Terminated
Recall initiated
22 Oct 2024
FDA classified
14 Nov 2024
Reported
20 Nov 2024
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
E. coli
Product category
Fish

Timeline

22 Oct 2024Recall initiated by company
14 Nov 2024Classified by FDA+23 days
20 Nov 2024Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potentially contaminated with E. coli O157:H7.

Some strains of E. coli, such as O157:H7, produce a toxin that can cause severe stomach cramps, bloody diarrhea and, in a small number of cases, kidney failure.

Product as listed by the FDA

154784 1 / 5LB IMPERIALFRESH PROC FAJITA GRN PEPRED PEP W All lot codes

Where it was distributed

Colorado

Colorado

Questions about this recall

Why was it recalled?

Potentially contaminated with E. coli O157:H7.

Which lots are affected?

All lot codes of the recalled products listed above produced between 10/8/2024 and 10/22/2024

Where was it sold?

Colorado

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 95622

This product is part of a recall event; the main page for the event is Item Number Pack/SZ Brand Description Lot Codes 082076 4/5 LBS recalled.

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