Wisco Pop Cherry Soda, 12 FL OZ. 355 ML, UPC 50037-32412. Handcrafted for Wisco pop Bev. Co. Madison, WI 53704
Summary
The FDA issued a Class II for Wisco Pop Cherry Soda, 12 FL OZ. 355 ML, UPC 50037-32412. Handcrafted for Wisco by Karben4 Brewing LLC. Reason: Cans of soda may contain yeast..
Details
Source
Food Recall
External ID
F-1103-2022
Action Date
2022-06-08
Status
Ongoing
Category
food
Product Description
Wisco Pop Cherry Soda, 12 FL OZ. 355 ML, UPC 50037-32412. Handcrafted for Wisco pop Bev. Co. Madison, WI 53704
Lot/Code Info: Lots: 030722.01 and 040822.02
Quantity Affected: 644 cases (24 cans per case)
Reason for Recall
Cans of soda may contain yeast.
Distribution
IL, MN, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-11
Company
Madison, 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 76 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Karben4 Brewing LLC has 4 FDA actions in our database, including 4 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 (Karben4 Brewing LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Karben4 Brewing LLC have FDA actions?
Karben4 Brewing LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1103-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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