D-LO's Delightful Gourmet Cheesecake, Pistachio, 142g single serve UPC 8 60007 40398 9, and 678g six serving UPC 8 6000
Summary
The FDA issued a Class I for D-LO's Delightful Gourmet Cheesecake, Pistachio, 142g single serve UPC 8 60007 by D-lo's Gourmet Cheesecake. Reason: Undeclared wheat, soy, colors (yellow 5 and blue 1), incomplete contains statement.
Details
Source
Food Recall
External ID
F-1224-2024
Action Date
2024-05-15
Status
Terminated
Category
food
Product Description
D-LO's Delightful Gourmet Cheesecake, Pistachio, 142g single serve UPC 8 60007 40398 9, and 678g six serving UPC 8 60007 40395 8, both serving sizes in clear plastic container with hinged lid
Lot/Code Info: Best by date of 04/09/2024
Quantity Affected: 8 retail units total
Reason for Recall
Undeclared wheat, soy, colors (yellow 5 and blue 1), incomplete contains statement
Distribution
MI
Type: Voluntary: Firm initiated
Recall Initiated: 2024-04-08
Company
Detroit, MI
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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (D-lo's Gourmet Cheesecake) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does D-lo's Gourmet Cheesecake have FDA actions?
This is the only FDA action we have on record for D-lo's Gourmet Cheesecake in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1224-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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