Lush Lavender & Wildberry Spritz is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold
Summary
The FDA issued a Class III for Lush Lavender & Wildberry Spritz is a non-alcoholic cocktail mixer. Product is by Urban River Spirits. Reason: Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing..
Details
Source
Food Recall
External ID
F-1626-2024
Action Date
2024-08-14
Status
Terminated
Category
food
Product Description
Lush Lavender & Wildberry Spritz is a non-alcoholic cocktail mixer. Product is packaged in glass 750ml bottle and sold under brand Urban River Spirits. Label has listed instructions as Shake Well Refrigerated After Opening.
Lot/Code Info: None
Quantity Affected: 3876 bottles total for all products
Reason for Recall
Firm made non-alcoholic drink mixer in an unlicensed and uninspected facility. The product safety is concerned due to potential under-processing.
Distribution
Distributed in Arizona, Idaho, California, Colorado, Iowa, Florida, Oregon, Nevada, New Jersey, Texas, and Washington.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-01
Company
Forest Grove, OR
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 200 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Urban River Spirits has 24 FDA actions in our database, including 24 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Urban River Spirits) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Urban River Spirits have FDA actions?
Urban River Spirits has 24 FDA actions in our database, including 24 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1626-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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