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Voluntary

Brite Beverage

Recall Reason

Adulterated: Prohibited Product; Other

Recall Overview

The Department of Cannabis Control (DCC) is issuing this notice of voluntary recall for multiple Brite beverage products due to inaccurate product type on the labels, inability to establish the licensee is manufacturing with good manufacturing practices (GMP), and because the products exceed the per package concentration limit for THC. These products are acidified beverages and are therefore prohibited.

Business Recall Date
5/14/2025
DCC Recall Publication Date
5/15/2025
Recall Type
Voluntary
Product Type
Beverage
Product Description
Brite Beverage
Legal Business Name
United Medical Alliance LLC
Legal Business License Number
C11-0000687-LIC
Manufactured By
United Medical Alliance LLC
Manufactured By License Number
DCC-10003638
Business Website
https://www.britelabs.com/

Product Details

This recall applies to the following Brite Beverage products:

There are no records to display

Locations where the recalled product was sold

There are no records to display

What consumers need to know

If you purchased this product:

  • If you are experiencing symptoms or any adverse reactions, contact your physician immediately.
  • Check your package for the UID and batch number(s) above.
  • If the numbers match, dispose of the product or return it to the retailer for proper disposal.

What licensees need to know

DCC sent notices to all licensees with this product in their inventory with instructions about responding to this recall. Contact our team at recalls@cannabis.ca.gov if you have any questions.