The Recall Desk
SevereFDA (Drugs)·D-0987-2019·Announced 2019-03-13

Sunstone Organics Recalls White Vein Kratom Powder Due to Salmonella

Sunstone Organics is recalling White Vein Kratom powder in 25, 50, and 100-gram packages because samples tested positive for Salmonella.

What this means for you

Illness, injury, or structural failure has been reported. 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 score of 4 per the rubric. Additionally, Salmonella is a high-risk pathogen.

Plain-English summary

Todd Holiday dba Sunstone Organics is recalling White Vein Kratom powder in 25-gram, 50-gram, and 100-gram packages. The recall involves Lot #119, with a total quantity of 250 kilograms. The product was distributed in California, Nebraska, Oregon, and Washington.

The recall was initiated because analysis of samples was positive for Salmonella. This is a microbial contamination issue affecting non-sterile products.

Consumers who purchased this product should stop using it and contact Sunstone Organics at 541-972-3327 for further instructions.

The recalled product

Product
White Vein Kratom, packaged in a) 25 gram powder (UPC 00859667007316), b) 50 gram powder (UPC 00859667007323), c) 100 gram powder (UPC 00859667007330), Sunstone Organics Springfield, Oregon 97473, 541-972-3327.

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

Distributed in 4 states:

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 →