Recall record at a glance
| Official record | F-1988-2014 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Prep Enterprises LLC |
| Report date | Jun 11, 2014 |
| Recall initiation date | May 1, 2014 |
| Quantity | 155,470 units |
| Location | Carlsbad, CA, United States |
Official product description
CAPTAIN KRATOM GOLD XL 30 Grams MAENG DA CAPSULES CAPTAIN KRATOM GOLD 15 GRAMS MAENG DA CAPSULES CAPTAIN KRATOM PREMIUM THAI POWDER 15 Grams CAPTAIN KRATOM PREMIUM BALI CAPSULES 15 Grams CAPTAIN VIETNAM KRATOM PREMIUM PLATINUM STRAIN 15 GRAMS CAPTAIN KRATOM PREMIUM THAI LEAF 15 Grams CAPTAIN KRATOM 30 grams Thai Capsules XL CAPTAIN KRATOM PREMIUM THAI CAPSULES 8 Grams MINI CAPTAIN KRATOM PREMIUM THAI RESIN 6 Grams CAPTAIN VIETNAM KRATOM PREMIUM PLATINUM STRAIN 30 GRAMS
Why the product was recalled
Prep Enterprises is recalling Captain Kratom, Arena Ethnobotanicals and Kratom Pro products because they may be contain Kratom (mitragyna speciosa).
Distribution information
The products were sold to wholesale distributors in the following states: Alabama, Arizona, California, Texas, Washington, Nevada, New York, Illinois, Missouri, Kentucky, Florida, Oklahoma, Idaho, Colorado, Wisconsin, Massachusetts, and Ohio. Wordwide to Canada.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.