Sterile Cannabidiol (CBD) 50mg/mL, 10mL vial
FDA Recall #D-1328-2020 — Class II — May 11, 2020
Product Description
Sterile Cannabidiol (CBD) 50mg/mL, 10mL vial
Reason for Recall
Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin
Recalling Firm
BIOTA Biosciences LLC — Seattle, WA
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Drugs
Product Quantity
N/A
Distribution
Nationwide within the United States and New Zealand
Code Information
Lot #: 101019P, 1010019P,10102019P, Exp. Date 10/10/2021
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated