Sunstone Organics Recalls White Vein Kratom Capsules Due to Salmonella
Sunstone Organics is recalling White Vein Kratom capsules in 20, 60, and 150-count bottles because samples tested positive for Salmonella.
The agency’s classification
FDA (Drugs): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class I, which mandates a minimum severity score of 4 according to the rubric, and involves a high-risk pathogen (Salmonella).
Plain-English summary
Todd Holiday dba Sunstone Organics is recalling White Vein Kratom capsules in 20-count, 60-count, and 150-count packages. The recall is due to microbial contamination, as analysis of samples was positive for Salmonella.
The affected product is identified as Lot #119. The capsules were distributed in California, Nebraska, Oregon, and Washington. Specific UPCs for the affected packages are 00859667007347, 00859667007354, and 00859667007361.
Consumers who have purchased these products should stop using them and contact the recalling firm for further instructions.
The recalled product
- Product
- White Vein Kratom, packaged in a) 20 count capsules (UPC 00859667007347), b) 60 count capsules (UPC 00859667007354), c) 150 count capsules (UPC 00859667007361), Sunstone Organics Springfield, Oregon 97473 541-972-3327.
- Manufacturer
- Todd Holiday dba Sunstone Organics
- Category
- Food — Dietary Supplement
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot #119
Distribution
Part of a larger recall action
This product is one of 4 recalled by Todd Holiday dba Sunstone Organics under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 4 products in this recall →Related recalls
Same manufacturer · Todd Holiday dba Sunstone Organics
See all →- SevereSunstone Organics Recalls White Vein Kratom Powder Due to Salmonella
FDA (Drugs) · 2019-03-13
- SevereSunstone Organics Recalls Maeng Da Kratom Capsules Due to Salmonella Contamination
FDA (Drugs) · 2019-03-13
- SevereSunstone Organics Recalls Maeng Da Kratom Powder Due to Salmonella Contamination
FDA (Drugs) · 2019-03-13
Same hazard · salmonella
See all →- SevereBerlin Seeds Recalls Alfalfa Sprouting Seeds for Potential E. coli and Salmonella
FDA (Food) · 2026-10-14
- CriticalTodd's Seeds Alfalfa and Mung Bundle Recalled for E. coli and Salmonella Risk
FDA (Food) · 2026-10-07
- CriticalTodd's Seeds Salad Sprouting Mixture Recalled for E. coli and Salmonella Risk
FDA (Food) · 2026-10-07
- CriticalTodd's Seeds Sprouting Seed Mix Recalled for E. coli and Salmonella Risk
FDA (Food) · 2026-10-07
- CriticalTodd's Seeds Broccoli & Friends Sprouting Seed Mix Recalled for Contamination
FDA (Food) · 2026-10-07
Similar recalls
- CriticalTriangle Pharmanaturals Recalls Kratom Products Due to Salmonella Contamination Risk
FDA (Food) · 2018-05-16
- CriticalTriangle Pharmanaturals Recalls Kratom Products Due to Salmonella Risk
FDA (Food) · 2018-05-16
- CriticalFDA Recalls Kratom Capsules Due to Potential Salmonella Contamination
FDA (Food) · 2018-03-28
- SevereTriangle Pharmanaturals Recalls Kratom Capsules Due to Salmonella Risk
FDA (Food) · 2018-05-16
- CriticalTriangle Pharmanaturals Recalls Chameleon Kratom Formula 51 Due to Salmonella Risk
FDA (Food) · 2018-05-16
- CriticalPdx Aromatics Recalls Kratom Capsules Due to Salmonella Contamination
FDA (Food) · 2018-03-28