FDA Recall D-0988-2019
Todd Holiday dba Sunstone Organics · Springfield, OR
Class I — life-threatening Terminated 1462 days on record
Highest impact — Class I recall — FDA determination of strong likelihood of serious adverse health consequence or death.
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.
Reason for recall
MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS: Analysis of samples were positive for Salmonella.
Recall record
- Recall number
D-0988-2019- Classification
- Class I
- Status
- Terminated
- Voluntary or mandated
- Voluntary: Firm initiated
- Firm notification
- Telephone
- Distribution
- California, Nebraska, Oregon, Washington
- Recall initiated
- 2019-02-13
- Classified by FDA Center
- 2019-03-11
- FDA published
- 2019-03-13
- Terminated
- 2023-02-14
- Recalling firm
- Todd Holiday dba Sunstone Organics
- Firm location
- Springfield, OR