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H-0236-2025Class II

UNFI General Corporate

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
UNFI General Corporate
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-07-16
Distribution
NJ, NY, MD, DC, PA
Firm state
RI
Product quantity
213 cases (total)
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

May be contaminated with fluid from a reach truck

Product description

1. WLD HRVST OG2 CAULIFLOWER

Code / lot info

1. UPC: 07-11535-51668 case code: 51668

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 →