Schweppes ZERO SUGAR GINGER ALE CAFFIENE FREE 7.5 FL OZ (221 mL) PRODUCED UNDER THE AUTHORITY OF DR. PEPPER/SEVEN UP, IN
Summary
The FDA issued a Class II for Schweppes ZERO SUGAR GINGER ALE CAFFIENE FREE 7.5 FL OZ (221 mL) PRODUCED UNDER by Pepsico Inc. Reason: During an internal investigation the firm discovered that product labeled as Zero Sugar contains full sugar product..
Details
Source
Food Recall
External ID
F-1120-2024
Action Date
2024-04-17
Status
Terminated
Category
food
Product Description
Schweppes ZERO SUGAR GINGER ALE CAFFIENE FREE 7.5 FL OZ (221 mL) PRODUCED UNDER THE AUTHORITY OF DR. PEPPER/SEVEN UP, INC., 5301 LEGACY DRIVE, PLANO, TX 75024 UPC 0 78000 02965 9
Lot/Code Info: May 20 24 MAY20240520VS02164 - MAY20240550VS02164
Quantity Affected: 233cs/6/4 pk cases (24 pk)
Reason for Recall
During an internal investigation the firm discovered that product labeled as Zero Sugar contains full sugar product.
Distribution
Product was shipped to the following states: MD, PA & WV
Type: Voluntary: Firm initiated
Recall Initiated: 2024-03-09
Company
Purchase, NY
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 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Pepsico Inc has 11 FDA actions in our database, including 11 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 (Pepsico Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Pepsico Inc have FDA actions?
Pepsico Inc has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1120-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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