CLASS I Food recall · Reported 12 Feb 2025 · FDA Enforcement Report
White Maeng da, kratom powder product packaged mylar recalled
Corepack Manufacturing is recalling White Maeng da, kratom powder product packaged mylar, distributed nationwide in the US. The recall was initiated on 12 Dec 2024 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0530-2025
- FDA event ID
- 95973
- Recalling firm
- Corepack Manufacturing, Orem, UT
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 12 Dec 2024
- FDA classified
- 5 Feb 2025
- Reported
- 12 Feb 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Salmonella
- Product category
- Energy Drinks
Timeline
| 12 Dec 2024 | Recall initiated by company | |
| 5 Feb 2025 | Classified by FDA | +55 days |
| 12 Feb 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Possible Salmonella contamination of affected product.
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
White Maeng da, kratom powder product packaged mylar resealable bags. 3 oz package, 80 bags per shipper box.
Where it was distributed
Throughout the United States.
Questions about this recall
Why was it recalled?
Possible Salmonella contamination of affected product.
Which lots are affected?
Lot #CP11122, Expired April 2024--not included on label--
Where was it sold?
Throughout the United States.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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