← FDA ENFORCEMENT
F-0530-2025Class I
COREPACK MANUFACTURING INC
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
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 MonitoringReason 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--
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 →