Mango Yogurt bar, ToYou Snacks Brand, 1.41 Oz/ 40 g, packaged in kraft laminated paper, 14 bars in 1 box.
Summary
The FDA issued a Class II for Mango Yogurt bar, ToYou Snacks Brand, 1.41 Oz/ 40 g, packaged in kraft laminated by Font Group of America Corp.. Reason: Undeclared Soy Allergen in various fruit and chocolate snack bars.
Details
Source
Food Recall
External ID
F-0812-2024
Action Date
2024-02-07
Status
Terminated
Category
food
Product Description
Mango Yogurt bar, ToYou Snacks Brand, 1.41 Oz/ 40 g, packaged in kraft laminated paper, 14 bars in 1 box.
Lot/Code Info: LOT: MY 05 EXP: 08/30/2024
Quantity Affected: 5670 units Total
Reason for Recall
Undeclared Soy Allergen in various fruit and chocolate snack bars
Distribution
United Sates
Type: Voluntary: Firm initiated
Recall Initiated: 2023-12-15
Company
Oakland, 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 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Font Group of America Corp. has 6 FDA actions in our database, including 6 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 (Font Group of America Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Font Group of America Corp. have FDA actions?
Font Group of America Corp. has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0812-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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