White Vein Kratom recall: Salmonella
White Vein Kratom, packaged in a) 25 gram powder (UPC 00859667007316), b) 50 gram powder (UPC 00859667007323), c) 100 gram powder (UPC…
Why was White Vein Kratom recalled?
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #119
- Product
- White Vein Kratom, packaged in a) 25 gram powder (UPC 00859667007316), b) 50 gram powder (UPC 00859667007323), c) 100 gram powder (UPC…
- Recalling firm
- Todd Holiday dba Sunstone Organics
- Quantity
- 250 Kilograms
- Distribution
- California, Nebraska, Oregon, Washington
- Recall date
- March 13, 2019
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)