FDA recall record
ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of March 11, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY
Reason
Tamarack Inc. is recalling Eclipse Kratom-containing powder products because it may be contaminated with Salmonella.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
ECLIPSE Kratom Premium Maeng Da, 40 count capsules and 2 oz bottles, Distributed by Tamarack Inc. Cheyenne, WY
Code information listed by FDA
All products on market.
Distribution and firm information
Recalling firm listed by FDA: Tamarack, Inc.
Firm location listed by FDA: Roy, UT, United States
Distribution reported by FDA: Distributed to retail stores in Utah. No foreign/VA/govt/military consignees.
Product quantity listed by FDA: 120 units
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.