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Sterile Curcumin 50mg/mL, 10 mL vial

FDA Recall #D-1330-2020 — Class II — May 11, 2020

Recall #D-1330-2020 Date: May 11, 2020 Classification: Class II Status: Terminated

Product Description

Sterile 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

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 #: 071219CCD, 0712019CCD, 07122019CCD, Exp. Date 7/12/2021

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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