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:
Locations where the recalled product was sold
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.
Grape Packaging
Watermelon Packaging
Horchata Packaging
Berry Packaging