The Recall Desk
SevereFDA (Drugs)·D-0988-2019·Announced 2019-03-13

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.

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 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.

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 →