Cafe' Intermezzo Party Time Torte 5.31 lbs Two Layers of rich vanilla cake filled with Butter cream! Decorated With spri
Summary
The FDA issued a Class II for Cafe' Intermezzo Party Time Torte 5.31 lbs Two Layers of rich vanilla cake fille by Epic Baking. Reason: Missing ingredient statement. Undeclared Milk, Egg, Wheat, Soy, Red 40, Red 3, Yellow 5, Yellow 6, Blue 1.
Details
Source
Food Recall
External ID
F-0599-2023
Action Date
2023-03-22
Status
Terminated
Category
food
Product Description
Cafe' Intermezzo Party Time Torte 5.31 lbs Two Layers of rich vanilla cake filled with Butter cream! Decorated With sprinkles.
Lot/Code Info: PTT010923 to PTT013123
Quantity Affected: 18 Tortes
Reason for Recall
Missing ingredient statement. Undeclared Milk, Egg, Wheat, Soy, Red 40, Red 3, Yellow 5, Yellow 6, Blue 1
Distribution
Product was shipped to the following states GA & TN
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-30
Company
Norcross, GA
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.
Epic Baking has 23 FDA actions in our database, including 23 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 (Epic Baking) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Epic Baking have FDA actions?
Epic Baking has 23 FDA actions in our database, including 23 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0599-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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