CLASS I Drug recall · Reported 13 Mar 2019 · FDA Enforcement Report
Maeng Da Kratom recalled by Todd Holiday
Todd Holiday is recalling Maeng Da Kratom, distributed in California, Nebraska, Oregon, Washington. The recall was initiated on 13 Feb 2019 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0986-2019
- FDA event ID
- 82247
- Recalling firm
- Todd Holiday, Springfield, OR
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 13 Feb 2019
- FDA classified
- 11 Mar 2019
- Reported
- 13 Mar 2019
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Salmonella
Timeline
| 13 Feb 2019 | Recall initiated by company | |
| 11 Mar 2019 | Classified by FDA | +26 days |
| 13 Mar 2019 | Published in enforcement report | +2 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
Maeng Da Kratom, packaged in a) 25 gram powder (UPC 00859667007118), b) 50 gram powder (UPC 00859667007125), c) 100 gram powder (UPC 00859667007132), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
Where it was distributed
California, Nebraska, Oregon, Washington
Questions about this recall
Why was it recalled?
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Which lots are affected?
Lot #124A
Where was it sold?
California, Nebraska, Oregon, Washington
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
3 other products · FDA event 82247This product is part of a recall event; the main page for the event is White Vein Kratom recalled by Todd Holiday.
| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS I | White Vein Kratom recalled by Todd Holiday | Todd Holiday | Salmonella | 4 states | |
| CLASS I | White Vein Kratom recalled by Todd Holiday | Todd Holiday | Salmonella | 4 states | |
| CLASS I | Maeng Da Kratom recalled by Todd Holiday | Todd Holiday | Salmonella | 4 states |
More recalls from Todd Holiday
All 4| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Maeng Da Kratom recalled by Todd Holiday | Todd Holiday | Salmonella | 4 states |
| Drug | CLASS I | White Vein Kratom recalled by Todd Holiday | Todd Holiday | Salmonella | 4 states |
| Drug | CLASS I | White Vein Kratom recalled by Todd Holiday | Todd Holiday | Salmonella | 4 states |