US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 11, 2020 (6 years ago)

Sterile Cannabidiol (CBD) 50mg/mL, 10mL 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) 50mg/mL, 10mL vial

Recalling firm
BIOTA Biosciences LLC
Origin
WA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1328-2020

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

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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

BIOTA Biosciences LLC D-1326-2020