Coffee + Lemonade Concentrate + Vanilla Syrup Canned Beverage packaged under the following brands and sizes: 1. Knowl
Summary
The FDA issued a Class II for Coffee + Lemonade Concentrate + Vanilla Syrup Canned Beverage packaged under the by Snapchill, LLC. Reason: Potential under-processing..
Details
Source
Food Recall
External ID
F-1512-2024
Action Date
2024-07-24
Status
Terminated
Category
food
Product Description
Coffee + Lemonade Concentrate + Vanilla Syrup Canned Beverage packaged under the following brands and sizes: 1. Knowledge Perk "The Ace" Coffee Shandy, 12 oz. UPC 8 10149-37100 4.
Lot/Code Info: Cans with Expiration dates between June 16, 2024 and April 16, 2025.
Quantity Affected: 549,146 cans total
Reason for Recall
Potential under-processing.
Distribution
Nationwide. Outside the US: Canada
Type: Voluntary: Firm initiated
Recall Initiated: 2024-06-17
Company
Green Bay, WI
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 47 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Snapchill, LLC has 20 FDA actions in our database, including 20 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Snapchill, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Snapchill, LLC have FDA actions?
Snapchill, LLC has 20 FDA actions in our database, including 20 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1512-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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