Powerade Zero Mixed Berry - 20 oz PET bottles 24 variety pack, 8 bottles of Powerade Grape within the variety pack.
Summary
The FDA issued a Class II for Powerade Zero Mixed Berry - 20 oz PET bottles 24 variety pack, 8 bottles of Powe by THE COCA-COLA COMPANY. Reason: The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring..
Details
Source
Food Recall
External ID
F-1111-2024
Action Date
2024-04-10
Status
Terminated
Category
food
Product Description
Powerade Zero Mixed Berry - 20 oz PET bottles 24 variety pack, 8 bottles of Powerade Grape within the variety pack.
Lot/Code Info: Lot Codes 0013098209, 0013111742, 0013111657, 0013119902 Expiration date: NOV1124AMC
Quantity Affected: 387 cases
Reason for Recall
The potential presence of a foreign metal object in the product, i.e. a stainless-steel ring.
Distribution
U.S. distribution to 760 consignees in SC and FL.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-27
Company
Auburndale, FL
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 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.
THE COCA-COLA COMPANY 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 (THE COCA-COLA COMPANY) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does THE COCA-COLA COMPANY have FDA actions?
THE COCA-COLA COMPANY 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-1111-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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