Premium Grapenut Special, packaged in paper and plastic containers in sizes 3 Gallons, half gallons, and quarts. Keep Fr
Summary
The FDA issued a Class II for Premium Grapenut Special, packaged in paper and plastic containers in sizes 3 Ga by Today's Frozen Desserts, Inc.. Reason: Undeclared Yellow 5 & Yellow 6.
Details
Source
Food Recall
External ID
F-0030-2025
Action Date
2024-10-23
Status
Terminated
Category
food
Product Description
Premium Grapenut Special, packaged in paper and plastic containers in sizes 3 Gallons, half gallons, and quarts. Keep Frozen
Lot/Code Info: 00177240B, 00185240B, 00209240B, 00247240B, 00262240B. Expiration Date: 6/13/2025-9/13/2025
Quantity Affected: Total of 1,363 of all 5 flavors and Qt, Half Gal and 3 Gal sizes
Reason for Recall
Undeclared Yellow 5 & Yellow 6
Distribution
Product is distributed within the state of Florida
Type: Voluntary: Firm initiated
Recall Initiated: 2024-09-16
Company
Miami, 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 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Today's Frozen Desserts, Inc. has 5 FDA actions in our database, including 5 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 (Today's Frozen Desserts, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Today's Frozen Desserts, Inc. have FDA actions?
Today's Frozen Desserts, Inc. has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0030-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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