YoCrunch Vanilla Lowfat Yogurt with M&Ms 6 oz (170g) UPC 046675000792 packaged in plastic cup with self-contained plast
Summary
The FDA issued a Class II for YoCrunch Vanilla Lowfat Yogurt with M&Ms 6 oz (170g) UPC 046675000792 packaged by DANONE US LLC. Reason: Undeclared wheat.
Details
Source
Food Recall
External ID
F-0611-2023
Action Date
2023-03-22
Status
Terminated
Category
food
Product Description
YoCrunch Vanilla Lowfat Yogurt with M&Ms 6 oz (170g) UPC 046675000792 packaged in plastic cup with self-contained plastic dome attached on top, 12 cups per case
Lot/Code Info: Best if Used by: March 16, 2023
Quantity Affected: 240 cases
Reason for Recall
Undeclared wheat
Distribution
Ohio, Pennsylvania, Kentucky, North Carolina, South Carolina
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-22
Company
White Plains, 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 488 food recalls issued in the same week, part of 204 food-related FDA actions this month.
DANONE US LLC has 16 FDA actions in our database, including 16 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 (DANONE US LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does DANONE US LLC have FDA actions?
DANONE US LLC has 16 FDA actions in our database, including 16 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0611-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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