Class ITerminatedVoluntary: Firm initiated

Hy-Vee: food recall H-0114-2025

Hy-Vee of West Des Moines, IA recalled Spicy Shrimp Poke Bowl. Reason: Potential contamination with Listeria monocytogenes. The FDA listed it as Class I in its Enforcement Report dated Jul 2, 2025.

Record status as published: Terminated (terminated Jul 30, 2025). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
Spicy Shrimp Poke Bowl
Product quantity
122.5 cases total
Reason for recall
Potential contamination with Listeria monocytogenes
Codes, lots and dates on the package
02-86882-00000
Distribution pattern
Retail locations throughout the Midwest
Recalling firm
Hy-Vee, West Des Moines, IA
Classification
Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmJun 5, 2025
Classified by the FDAJun 25, 2025
Published in the Enforcement ReportJul 2, 2025
TerminatedJul 30, 2025

Other products in the same recall event

The FDA groups related products under one recall event (event 97065).

All food recall records

OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.

Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0114-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
  • Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.