Club 13 Kratom Maeng Da Red capsules; 5, 25, 50, 100, 120 capsule bottles, and Club 13 Kratom…
Recalling firm: Club 13 Enterprises Warehouse
Samples of Maeng Da red powder were tested and resulted positive for Salmonella.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 25, 2019.
Check your package
Compare the exact product and package details with the label you have.
FDA code information
Lots # MRMD013018, MRMD013118, MRMD020118, MRMD020518, MRMD022318, MRMD022718, MRMD030118, MRMD030218, and MRMD030618.
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
Club 13 Kratom Maeng Da Red capsules; 5, 25, 50, 100, 120 capsule bottles, and Club 13 Kratom Maeng Da Red capsules in bulk bags.
Original FDA recall reason
Samples of Maeng Da red powder were tested and resulted positive for Salmonella.
Recall details
- Recall number
- F-1120-2018
- Event ID
- 79716
- FDA status
- Terminated
- Initiated
- Mar 31, 2018
- Reported
- Apr 25, 2018
- Classified
- Apr 20, 2018
- Terminated
- Mar 25, 2019
- Quantity
- 7,683 units and 128 kg of capsules in bulk bags
- Location
- Saint Augustine, FL, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
U.S. consignees only.
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.