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ECLIPSE Kratom Premium Maeng Da recall
Recalled by Tamarack, Inc. · Roy, UT, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY
Quantity: 120 units
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
All products on market.
Where it was sold
Utah Virginia
FDA's distribution note: Distributed to retail stores in Utah. No foreign/VA/govt/military consignees.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Tamarack, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 19, 2018
- In FDA report of
- Apr 11, 2018
- Terminated
- Mar 11, 2020
- FDA recall number
- F-0992-2018 · event 79565
- Official record
- FDA enforcement report search
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