Sunstone Organics Recalls Maeng Da Kratom Capsules Due to Salmonella Contamination
Sunstone Organics is recalling Maeng Da 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 agency classification is FDA Class I, which mandates a minimum severity score of 4 per the rubric, and the presence of Salmonella is a high-risk pathogen.
Plain-English summary
Todd Holiday dba Sunstone Organics is recalling Maeng Da 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 Lot #124A. The recall covers products distributed in California, Nebraska, Oregon, and Washington. The specific UPCs for the affected packages are 00859667007149 (20 count), 00859667007156 (60 count), and 00859667007163 (150 count).
Consumers who have purchased these specific products should stop using them and contact Sunstone Organics at 541-972-3327 for further instructions.
The recalled product
- Product
- Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 150 count capsules (UPC 00859667007163) , Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
- Manufacturer
- Todd Holiday dba Sunstone Organics
- Category
- Drug — 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 #124A
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.
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