Class II · Moderate risk Terminated
Sterile Cannabidiol (CBD) 50mg/mL, 10mL vial
Reason 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
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin
What was recalled
Sterile Cannabidiol (CBD) + Curcumin 50mg/mL, 10 mL vial
- Recalling firm
- BIOTA Biosciences LLC
- Origin
- WA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1329-2020
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Cannabidiol recalls
See all
Class II · Moderate risk Terminated
Sterile Cannabidiol (CBD) 4mg/mL, 10mL vial
Reason Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin
Get an alert if your medication is recalled
Tell us which medications you take. If the FDA recalls one, we email you - in plain English, with what to do. Free.