Class ITerminatedVoluntary: Firm initiated
COREPACK MANUFACTURING INC: food recall F-0530-2025
COREPACK MANUFACTURING INC of Orem, UT recalled White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz package, 80 bags per shipper box. Reason: Possible Salmonella contamination of affected product. The FDA listed it as Class I in its Enforcement Report dated Feb 12, 2025; distribution: nationwide.
Record status as published: Terminated (terminated Jun 20, 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
- White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz package, 80 bags per shipper box.
- Product quantity
- 5520 units
- Reason for recall
- Possible Salmonella contamination of affected product.
- Codes, lots and dates on the package
- Lot #CP11122, Expired April 2024--not included on label--
- Distribution pattern
- Throughout the United States.
- Recalling firm
- COREPACK MANUFACTURING INC, Orem, UT
- 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
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Dec 12, 2024 |
| Classified by the FDA | Feb 5, 2025 |
| Published in the Enforcement Report | Feb 12, 2025 |
| Terminated | Jun 20, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0530-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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