Exact FDA event identifier

Event 79565

1 recalled-product record grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: March 19, 2018
Product types: Food
Classifications: Class I
Statuses: Terminated
Recalling firm wording: Tamarack, Inc.

Dossier provenance

Source snapshots represented here

openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

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

F-0992-2018

Recall number: F-0992-2018
Initiated: March 19, 2018
Classification: Class I
Status: Terminated
Recalling firm: Tamarack, Inc.
Quantity: 120 units

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0

contaminated with Salmonella

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

All products on market.

Distribution pattern

Distributed to retail stores in Utah. No foreign/VA/govt/military consignees.