JSJ DMC Leaf Cake 3.35 oz (95g) 28 units per case produced date: 2022/11/08
Summary
The FDA issued a Class I for JSJ DMC Leaf Cake 3.35 oz (95g) 28 units per case produced date: 2022/11/08 by Titans Global Inc.. Reason: Product was found to have the presence of egg, which is not declared on the label..
Details
Source
Food Recall
External ID
F-0412-2023
Action Date
2023-03-15
Status
Terminated
Category
food
Product Description
JSJ DMC Leaf Cake 3.35 oz (95g) 28 units per case produced date: 2022/11/08
Lot/Code Info: Lot code: 20221108B
Quantity Affected: 12,432 units total
Reason for Recall
Product was found to have the presence of egg, which is not declared on the label.
Distribution
Distributed to 5 retail locations locally within the state of CA.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-02-06
Company
City Of Industry, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Titans Global Inc. has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Titans Global Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Titans Global Inc. have FDA actions?
Titans Global Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0412-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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