ECLIPSE Kratom Premium Maeng Da
Recalling firm: Tamarack, Inc.
Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with 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 11, 2020.
Check your package
Compare the exact product and package details with the label you have.
FDA code information
All products on market.
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY
Original FDA recall reason
Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.
Recall details
- Recall number
- F-0992-2018
- Event ID
- 79565
- FDA status
- Terminated
- Initiated
- Mar 19, 2018
- Reported
- Apr 11, 2018
- Classified
- Apr 4, 2018
- Terminated
- Mar 11, 2020
- Quantity
- 120 units
- Location
- Roy, UT, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Visit
Where it was distributed
Distributed to retail stores in Utah. No foreign/VA/govt/military consignees.
Data updated September 16, 2026. View official FDA data ↗
Follow official FDA and manufacturer guidance.