FDA recall D-1329-2020

Product

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

Reason for recall

Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA: Product contains unapproved Cannabidiol and Curcumin

Distribution

Nationwide within the United States and New Zealand

Key facts

Status

Terminated

Initiation date

2020-05-11

Report date

2020-07-01

Termination date

2020-12-03

Voluntary/Mandated

Voluntary: Firm initiated

Location

Seattle, WA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1329-2020