Corepack Manufacturing Inc food recall: White Maeng da
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 95973
- Recall initiated
- Dec 12, 2024
- Classified by FDA
- Feb 5, 2025
- Posted in Enforcement Report
- Feb 12, 2025
- Terminated
- Jun 20, 2025
- Recalling firm
- COREPACK MANUFACTURING INC
- Firm location
- Orem, UT, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Letter
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Possible Salmonella contamination of affected product.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Dec 12, 2024. FDA classified it 55 days later, on Feb 5, 2025. Distribution reported by FDA: Throughout the United States.
Recalled products (1)
F-0530-2025 Class I Terminated
White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz package, 80 bags per shipper box.
Codes / lots: Lot #CP11122, Expired April 2024--not included on label--
Quantity: 5520 units
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 95973
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.