Sterile Cannabidiol (CBD) 50mg/mL, 10mL vial
Reported: July 1, 2020 Initiated: May 11, 2020 #D-1328-2020
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
Details
- Recalling Firm
- BIOTA Biosciences LLC
- Units Affected
- N/A
- Distribution
- Nationwide within the United States and New Zealand
- Location
- Seattle, WA
Frequently Asked Questions
What product was recalled? ▼
Sterile Cannabidiol (CBD) 50mg/mL, 10mL vial. Recalled by BIOTA Biosciences LLC. Units affected: N/A.
Why was this product recalled? ▼
Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 1, 2020. Severity: Moderate. Recall number: D-1328-2020.
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