D-0988-2019 Class I Terminated
FDA drug recall D-0988-2019 was initiated by Todd Holiday dba Sunstone Organics on February 13, 2019 and is designated Class I. Reason for recall: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella. The recall status is terminated (terminated February 14, 2023). Affected quantity: N/A.
Recall Details
- Product Type
- Drugs
- Report Date
- March 13, 2019
- Initiation Date
- February 13, 2019
- Termination Date
- February 14, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- N/A
Product Description
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.
Reason for Recall
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Distribution Pattern
California, Nebraska, Oregon, Washington
Code Information
Lot #119