Food recall: EARTH KRATOM TRAINWRECK 150 CAPSULES (UPC: 908193737324) (50 UNITS/CASE) and 300 CAPSULES (UPC: 005821990011) (25 UNITS/
Fire Distributors Plus LLC (Hallandale Beach, FL) initiated this food recall on 18 May 2023; FDA lists 2 product records under event 92387, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 53% of the 478 food enforcement events initiated in 2023 carry the same class.
Status: Terminated, terminated 29 Aug 2023. Initiation: voluntary: firm initiated. This is the only enforcement event on this register for Fire Distributors Plus LLC.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Fire Distributors Plus LLC, Hallandale Beach, FL.
Reason for recall
"Products contain kratom, an unapproved food additive."
Distribution
"U.S. distribution only. No foreign distribution."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1000-2023 | 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. | 26,500 pouches of 150 count and 17,025 pouches of 300 count | Class II | Terminated | 28 Jun 2023 |
| F-1001-2023 | EARTH KRATOM RED MAENG DA KRATOM 65 CAPSULES (UPC: 212223242796) (100 UNITS/CASE). DISTRIBUTED BY FIRE WHOLESALE. Ingredients: Mitragyna speciosa leaf, purified water, vegetable magnesium stearate, and gelatin capsules. | 31,600 pouches | Class II | Terminated | 28 Jun 2023 |
Context
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Products contain kratom, an unapproved food additive."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "U.S. distribution only. No foreign distribution."
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 29 Aug 2023. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.