Check the Batch
Class IITerminated in FDA datasetRecall initiated May 18, 2023

Earth Kratom Trainwreck 150 Capsules (

Recalling firm: Fire Distributors Plus LLC

Why it was recalled

Products contain kratom, an unapproved food additive.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 29, 2023.

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Compare the exact product and package details with the label you have.

ProductEARTH KRATOM TRAINWRECK 150 CAPSULES (UPC: 908193737324) (50 UNITS/CASE) and 300 CAPSULES (UPC: 005821990011) (25 UNITS/CASE). DISTRIBUTED BY FIRE WHOLESALE. Ingredients: Mitragyna speciosa leaf, purified water, vegetable magnesium stearate, and gelatin capsules.
UPC005821990011, 908193737324

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Full FDA record and distribution details

Original product description

EARTH KRATOM TRAINWRECK 150 CAPSULES (UPC: 908193737324) (50 UNITS/CASE) and 300 CAPSULES (UPC: 005821990011) (25 UNITS/CASE). DISTRIBUTED BY FIRE WHOLESALE. Ingredients: Mitragyna speciosa leaf, purified water, vegetable magnesium stearate, and gelatin capsules.

Extracted codes and context

TypeCode / valueContext
UPC005821990011INWRECK 150 CAPSULES (UPC: 908193737324) (50 UNITS/CASE) and 300 CAPSULES (UPC: 005821990011) (25 UNITS/CASE). DISTRIBUTED BY FIRE WHOLESALE. Ingredients: Mitragyna speciosa leaf, purified water, vegetable magnes
UPC908193737324EARTH KRATOM TRAINWRECK 150 CAPSULES (UPC: 908193737324) (50 UNITS/CASE) and 300 CAPSULES (UPC: 005821990011) (25 UNITS/CASE). DISTRIBUTED BY FIRE WHOLESALE. Ingredients: Mitr

Original FDA recall reason

Products contain kratom, an unapproved food additive.

Recall details

Recall number
F-1000-2023
Event ID
92387
FDA status
Terminated
Initiated
May 18, 2023
Reported
Jun 28, 2023
Classified
Jun 22, 2023
Terminated
Aug 29, 2023
Quantity
26,500 pouches of 150 count and 17,025 pouches of 300 count
Location
Hallandale Beach, FL, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

U.S. distribution only. No foreign distribution.

FDA source record · F-1000-2023

Data updated September 16, 2026. View official FDA data ↗

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