White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz package, 80 bags per shipper box.
Summary
The FDA issued a Class I for White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz pack by COREPACK MANUFACTURING INC. Reason: Possible Salmonella contamination of affected product..
Details
Source
Food Recall
External ID
F-0530-2025
Action Date
2025-02-12
Status
Terminated
Category
food
Product Description
White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz package, 80 bags per shipper box.
Lot/Code Info: Lot #CP11122, Expired April 2024--not included on label--
Quantity Affected: 5520 units
Reason for Recall
Possible Salmonella contamination of affected product.
Distribution
Throughout the United States.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-12
Company
Orem, UT
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (COREPACK MANUFACTURING INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does COREPACK MANUFACTURING INC have FDA actions?
This is the only FDA action we have on record for COREPACK MANUFACTURING INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0530-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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