VEGAN OAT; Van Leeuwen PUMPKIN CINNAMON ROLL; NON-DAIRY FROZEN DESSERT 14 oz, (414 ml); Est. Brooklyn 2008 ingredients:
Summary
The FDA issued a Class I for VEGAN OAT; Van Leeuwen PUMPKIN CINNAMON ROLL; NON-DAIRY FROZEN DESSERT 14 oz, (4 by Van Leeuwen Ice Cream LLC. Reason: Undeclared peanuts (allergen).
Details
Source
Food Recall
External ID
F-1739-2024
Action Date
2024-08-21
Status
Terminated
Category
food
Product Description
VEGAN OAT; Van Leeuwen PUMPKIN CINNAMON ROLL; NON-DAIRY FROZEN DESSERT 14 oz, (414 ml); Est. Brooklyn 2008 ingredients: oat milk (water, oats) coconut cream, cane sugar, brown sugar, unbleached wheat flour, tapioca syrup, pumpkin puree, coconut oil, cocoa butter, water, ginger, corn starch, vanilla extract, natural flavor, annatto (for color), sea salt, cinnamon, carob, quar, nutmeg contains: wheat, tree nuts (coconut) C7237-001 VAN LEEUWEN ICE CREAM LLC, BROOKLYN, NY, 11222, 718 701 1630, MANUFACTURED IN A FACILITY THAT HANDLES DAIRY, EGGS, TREE NUTS, PEANUTS, WHEAT AND SOY Product UPC: 850005872375
Lot/Code Info: Best by: 2026-04-03 Lot # 29V094
Quantity Affected: 8 pints
Reason for Recall
Undeclared peanuts (allergen)
Distribution
NY
Type: Voluntary: Firm initiated
Recall Initiated: 2024-07-29
Company
Brooklyn, NY
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 125 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Van Leeuwen Ice Cream LLC has 2 FDA actions in our database, including 2 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 (Van Leeuwen Ice Cream LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Van Leeuwen Ice Cream LLC have FDA actions?
Van Leeuwen Ice Cream LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1739-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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