Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC Cardboard Wrap Code: 7153700228, UPC Can Code: 7153700110
Summary
The FDA issued a Class II for Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC Cardboard Wrap Code: by KEURIG DR PEPPER. Reason: The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained.
Details
Source
Food Recall
External ID
F-0240-2022
Action Date
2021-12-08
Status
Terminated
Category
food
Product Description
Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC Cardboard Wrap Code: 7153700228, UPC Can Code: 7153700110
Lot/Code Info: Product Code Date: 12/16/2022 KDC
Quantity Affected: 7,849 cases
Reason for Recall
The company has received off flavor and off aroma complaints identified with the recalled lot. After analysis it was found that the products contained unlabeled sulfites.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-14
Company
Frisco, TX
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 48 food recalls issued in the same week, part of 204 food-related FDA actions this month.
KEURIG DR PEPPER has 7 FDA actions in our database, including 7 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 (KEURIG DR PEPPER) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does KEURIG DR PEPPER have FDA actions?
KEURIG DR PEPPER has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0240-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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