← FDA ENFORCEMENT
F-0530-2025Class I

COREPACK MANUFACTURING INC

Recalling firm
COREPACK MANUFACTURING INC
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-02-12
Distribution
Throughout the United States.
Firm state
UT
Product quantity
5520 units
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Possible Salmonella contamination of affected product.

Product description

White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz package, 80 bags per shipper box.

Code / lot info

Lot #CP11122, Expired April 2024--not included on label--

Other recalls SPEQ maps to Environmental Monitoring
2026-07-22Class IArgon Medical Devices, Inc2026-07-22Class IIOlympus Corporation of the Americas2026-07-22Class IIChiesi USA, Inc.2026-07-22Class IICareFusion 213, LLC
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.