← FDA ENFORCEMENT
F-0138-2025Class I
FreshPoint Denver, Incorporated
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
FreshPoint Denver, Incorporated
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2024-11-20
Distribution
Colorado
Firm state
CO
Product quantity
7 cases (5lbs ea case)
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental MonitoringReason for recall
Potentially contaminated with E. coli O157:H7.
Product description
154784 1 / 5LB IMPERIALFRESH PROC FAJITA GRN PEPRED PEP W All lot codes
Code / lot info
All lot codes of the recalled products listed above produced between 10/8/2024 and 10/22/2024
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →