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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Todd Holiday dba Sunstone Organics: Maeng Da and White Vein Kratom Recalled for Salmonella Contamination

Agency Publication Date: March 6, 2019
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Summary

Todd Holiday dba Sunstone Organics is recalling approximately 1,050 units (totaling 1,050 kilograms) of Maeng Da Kratom and White Vein Kratom in both powder and capsule forms. This recall was initiated after samples tested positive for Salmonella, a bacteria that can cause serious gastrointestinal illness. The affected products were distributed in California, Nebraska, Oregon, and Washington and were sold in various sizes ranging from 25-gram powders to 150-count capsules.

Risk

The products are contaminated with Salmonella, which can cause fever, diarrhea, nausea, vomiting, and abdominal pain. In vulnerable populations such as young children, the elderly, or those with weakened immune systems, Salmonella can lead to severe or life-threatening infections.

What You Should Do

  1. Check your product packaging for Maeng Da Kratom or White Vein Kratom from Sunstone Organics with the following lot numbers: Lot #124A (Maeng Da) or Lot #119 (White Vein).
  2. Verify the UPC codes on your packaging: Maeng Da Powder (00859667007118, 00859667007125, 00859667007132), Maeng Da Capsules (00859667007149, 00859667007156, 00859667007163), White Vein Powder (00859667007316, 00859667007323, 00859667007330), or White Vein Capsules (00859667007347, 00859667007354, 00859667007361).
  3. Immediately stop using any affected kratom products and dispose of them or return them to the place of purchase.
  4. Contact your healthcare provider or pharmacist for guidance if you have consumed these products and feel unwell.
  5. Contact Sunstone Organics at 541-972-3327 for specific questions regarding this recall or for refund information.
  6. Return any unused product to the pharmacy or retail location for a refund.
  7. For additional questions, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

💰Full Refund

Healthcare provider consultation and pharmacy return

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Maeng Da Kratom powder (25 gram)
Model:
D-0986-2019
UPC Codes:
00859667007118
Lot Numbers:
124A
Product: Maeng Da Kratom powder (50 gram)
Model:
D-0986-2019
UPC Codes:
00859667007125
Lot Numbers:
124A
Product: Maeng Da Kratom powder (100 gram)
Model:
D-0986-2019
UPC Codes:
00859667007132
Lot Numbers:
124A
Product: White Vein Kratom powder (25 gram)
Model:
D-0987-2019
UPC Codes:
00859667007316
Lot Numbers:
119
Product: White Vein Kratom powder (50 gram)
Model:
D-0987-2019
UPC Codes:
00859667007323
Lot Numbers:
119
Product: White Vein Kratom powder (100 gram)
Model:
D-0987-2019
UPC Codes:
00859667007330
Lot Numbers:
119
Product: White Vein Kratom capsules (20 count)
Model:
D-0988-2019
UPC Codes:
00859667007347
Lot Numbers:
119
Product: White Vein Kratom capsules (60 count)
Model:
D-0988-2019
UPC Codes:
00859667007354
Lot Numbers:
119
Product: White Vein Kratom capsules (150 count)
Model:
D-0988-2019
UPC Codes:
00859667007361
Lot Numbers:
119
Product: Maeng Da Kratom capsules (20 count)
Model:
D-0989-2019
UPC Codes:
00859667007149
Lot Numbers:
124A
Product: Maeng Da Kratom capsules (60 count)
Model:
D-0989-2019
UPC Codes:
00859667007156
Lot Numbers:
124A
Product: Maeng Da Kratom capsules (150 count)
Model:
D-0989-2019
UPC Codes:
00859667007163
Lot Numbers:
124A

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 82247
Status: Resolved
Manufacturer: Todd Holiday dba Sunstone Organics
Sold By: Sunstone Organics
Manufactured In: United States
Units Affected: 2 products (800 kilograms; 250 Kilograms)
Distributed To: California, Nebraska, Oregon, Washington
Agency Last Updated: March 11, 2019

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · FDA Press Release · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.