Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gal
Summary
The FDA issued a Class II for Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz c by Zarlengo Italian Ice. Reason: Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement..
Details
Source
Food Recall
External ID
H-0650-2026
Action Date
2026-04-15
Status
Completed
Category
food
Product Description
Zarlengo's Chocolate Chocolate Chip Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gallon bucket/pail and 2-gallon bucket/pail) , Net Wt. 6 fl oz cups - clear freezer grade and round Polyethylene terephthalate cup with peelable paper lid, laminated with heat-sealable plastic, 16 fl oz cups and 32 fl oz cups translucent freezer grade and round High-Density Polyethylene container with lid and 1-Gallon and 2-Gallon bucket/pail - white round food and freezer grade High-Density Polyethylene bucket/pail with tamper resistant lid.
Lot/Code Info: Lot Codes: 6 fl oz cups--- 03026, 00226, 05426, 05726 16 fl oz (or pint) -- 33825 32 fl oz-- 33825 1 gallon-- 03026
Quantity Affected: Total of 1,333 multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups, 1-gallon bucket/pail and 2-gallon bucket/pail)
Reason for Recall
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Distribution
IL, IN and TX
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-26
Company
Chicago Heights, IL
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 29 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Zarlengo Italian Ice has 3 FDA actions in our database, including 3 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 (Zarlengo Italian Ice) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Zarlengo Italian Ice have FDA actions?
Zarlengo Italian Ice has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0650-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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