ECLIPSE Kratom Premium Maeng Da recalled over Salmonella risk
- Recall date
- March 19, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Tamarack, Inc. recalls ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY
- Recall number
- F-0992-2018
- FDA classification
- Class I
- Brand / firm
- Tamarack, Inc.
- Sold / distributed
- Distributed to retail stores in Utah. No foreign/VA/govt/military consignees.
Why it was recalled
Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY
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