← FDA ENFORCEMENT
H-0114-2025Class I
Hy-Vee
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
Hy-Vee
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-07-02
Distribution
Retail locations throughout the Midwest
Firm state
IA
Product quantity
122.5 cases total
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental MonitoringReason for recall
Potential contamination with Listeria monocytogenes
Product description
Spicy Shrimp Poke Bowl
Code / lot info
02-86882-00000
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 →