PEANUT BUTTER/MAZAPAN, Ice-cream base, Natural Flavor, Artificial Color, sea salt., Distributed by PARADISE FLAVORS LLC,
Summary
The FDA issued a Class I for PEANUT BUTTER/MAZAPAN, Ice-cream base, Natural Flavor, Artificial Color, sea sal by Paradise Flavors LLC. Reason: Undeclared allergens: Milk, peanut, soy, and wheat..
Details
Source
Food Recall
External ID
F-0448-2024
Action Date
2023-11-22
Status
Terminated
Category
food
Product Description
PEANUT BUTTER/MAZAPAN, Ice-cream base, Natural Flavor, Artificial Color, sea salt., Distributed by PARADISE FLAVORS LLC, 4 OZ. Packaged in plastic pouch. Frozen.
Lot/Code Info: None
Quantity Affected: 210 units (pieces) from latest production
Reason for Recall
Undeclared allergens: Milk, peanut, soy, and wheat.
Distribution
Domestic distribution only, within state of Florida. No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-27
Company
Marathon, FL
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 145 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Paradise Flavors LLC has 39 FDA actions in our database, including 39 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 (Paradise Flavors LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Paradise Flavors LLC have FDA actions?
Paradise Flavors LLC has 39 FDA actions in our database, including 39 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0448-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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