← FDA ENFORCEMENT
H-0106-2025Class I

Hy-Vee

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 Monitoring
Reason for recall

Potential contamination with Listeria monocytogenes

Product description

Red Dragon Roll

Code / lot info

02-86811-00000

Other recalls SPEQ maps to Environmental Monitoring
2026-07-22Class IArgon Medical Devices, Inc2026-07-22Class IIChiesi USA, Inc.2026-07-22Class IICareFusion 213, LLC2026-07-22Class IIOlympus Corporation of the Americas
See all Environmental Monitoring recalls →

Data: U.S. FDA openFDA enforcement API. 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.