ECLIPSE Kratom Premium Maeng Da
Recalling firm: Tamarack, Inc.
Why it was recalled
Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.
The exact product
ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
All products on market.
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.
FDA source record · F-0992-2018
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.