Recall · openFDA Food Enforcement

ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz…: FDA Recall F-0992-2018

Agency action: Mar 19, 2018Record ID: F-0992-2018
View official source ↗

What happened

Original notice title

ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY, recall F-0992-2018

From the archived source record

Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class I
Recall initiated by
Voluntary: Firm initiated
Report date
Apr 11, 2018
Termination date in the archive
Mar 11, 2020
Source checked
Jul 16, 2026
Record revision
0e010374c15c

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY
Company
Tamarack, Inc.
Lot / identifier
All products on market.
Market / distribution
Distributed to retail stores in Utah. No foreign/VA/govt/military consignees.