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

Tamarack, INC. recalled ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY in a Class I action — the FDA's most serious tier, reserved for products with a reasonable probability of causing serious health consequences or death on Mar 19, 2018.

The recall was triggered by possible Salmonella contamination: "Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella." Salmonella is one of the most common causes of U.S. foodborne illness, with symptoms that typically appear within six hours to six days of exposure.

The product reached multiple states, recorded by the FDA as "Distributed to retail stores in Utah. No foreign/VA/govt/military consignees." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Roy, UT. The recall covers 120 units of product. The FDA has Terminated this recall (first reported Apr 11, 2018), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.