Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Raspberry Lemonade Natural & Artificial Flavor, 33.8 FL OZ
Summary
The FDA issued a Class II for Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Raspberry Lemonade by Abbott Laboratories. Reason: These products are being recalled due to the potential of leakage from the 1L container..
Details
Source
Food Recall
External ID
F-1344-2022
Action Date
2022-06-29
Status
Terminated
Category
food
Product Description
Pedialyte with Immune Support***+Zinc/Selenium & Magnesium***Raspberry Lemonade Natural & Artificial Flavor, 33.8 FL OZ (1.05 QT) 1L*** INGREDIENTS: WATER, DEXTROSE***Abbott Nutrition, Abbott Laboratories, Columbus, Ohio 43219-3034 USA
Lot/Code Info: 30289SG00, 30290SG00, 30291SG00, 30292SG00, 30293SG00, 30294SG00, 35409SG00, 35410SG00, 35411SG00, 35412SG00, 36435SG00, 36434SG00, 36433SG00, 36432SG00, 37444SG00, 37443SG00, 37442SG00, 37441SG00, 37440SG00, and 41129D500.
Quantity Affected: 121,918 (2-count cases)
Reason for Recall
These products are being recalled due to the potential of leakage from the 1L container.
Distribution
AL, AR, AZ, CA, CO, DE, FL, GA, IA, IL, IN, KS, KY, LA, MI, MO, MS, NC, NH, NY, OH, OR, PA, TN, TX, UT, VA and WI
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-03
Company
Columbus, OH
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 78 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Abbott Laboratories has 101 FDA actions in our database, including 86 recalls and 15 clearances.
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 (Abbott Laboratories) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Abbott Laboratories have FDA actions?
Abbott Laboratories has 101 FDA actions in our database, including 86 recalls and 15 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1344-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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