Crush Orange Soda, 24 Pack. 24 - 12 oz. cans. Caffeine Free. Contains No Juice. UPC 0 78000-01309 2. Produced under
Summary
The FDA issued a Class II for Crush Orange Soda, 24 Pack. 24 - 12 oz. cans. Caffeine Free. Contains No Juic by Pepsi Beverages, LLC. Reason: foreign material - plastic.
Details
Source
Food Recall
External ID
F-0314-2024
Action Date
2023-11-08
Status
Terminated
Category
food
Product Description
Crush Orange Soda, 24 Pack. 24 - 12 oz. cans. Caffeine Free. Contains No Juice. UPC 0 78000-01309 2. Produced under the Authority of Dr Pepper/Seven Up, Inc., 6425 Hall of Fame Lane, Frisco, TX 75034
Lot/Code Info: JUL2924XXXXMC10243, Best by Date July 29th 2024
Quantity Affected: 184 cases
Reason for Recall
foreign material - plastic
Distribution
MN
Type: Voluntary: Firm initiated
Recall Initiated: 2023-10-27
Company
Burnsville, MN
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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Pepsi Beverages, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Pepsi Beverages, LLC have FDA actions?
This is the only FDA action we have on record for Pepsi Beverages, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0314-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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