Key Takeaway
Sterile Cannabidiol (CBD) + Curcumin 50mg/mL, 10 mL vial by BIOTA Biosciences LLC was recalled on May 11, 2020. The hazard: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin
Sterile Cannabidiol (CBD) + Curcumin 50mg/mL, 10 mL vial
Description
Sterile Cannabidiol (CBD) + Curcumin 50mg/mL, 10 mL vial
Hazard / Reason
Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin
Class II: Product that may cause temporary or medically reversible health consequences.
Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.
Products Affected
Sterile Cannabidiol (CBD) + Curcumin 50mg/mL, 10 mL vial
DrugsCompany Information
BIOTA Biosciences LLC
Seattle, WA, United States
View all 5 recalls by BIOTA Biosciences LLC →Distribution
Nationwide within the United States and New Zealand
Related Recalls
Frequently Asked Questions
Is this recall still active?
Check the status badge at the top of this page. "Ongoing" means the recall is still active and you should follow the remedy instructions. "Completed" or "Terminated" means the recall process has concluded, though the safety issue remains relevant for any unrepaired products.
How do I check if my product is affected?
Compare the model number, lot code, serial number, or date range listed in the recall notice with the information on your product's label or packaging. For vehicles, check your VIN at NHTSA.gov/Recalls.
What remedy is available for this recall?
Check the remedy section above or contact the manufacturer directly for current remedy options.
Where can I find the original recall notice?
This recall was issued by FDA Drug. Visit the agency's official website for the original notice.