Skip to main content

Zarlengo Italian Ice Recall: Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.

United States

TerminatedClass II

Company
Zarlengo Italian Ice
Product
Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl…
Recall date
March 26, 2026
Terminated
July 14, 2026
Source
FDA

Reason for recall

Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-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 bucket/pail - white round food and freezer grade High-Density Polyethylene bucket/pail with tamper resistant lid. Not published in this source record Total of 757 multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/pail) Lot Codes: 6 fl oz cups--- 00226, 03026, 05426, 33825 16 fl oz (or pint) -- 33825 1 gallon--05726

Distribution

  • IL
  • IN and TX

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0651-2026
Event ID
98651
Status
Terminated
Classification
Class II
Company
Zarlengo Italian Ice
Product description
Zarlengo's Chocolate Gelato packaged in multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-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 bucket/pail - white round food and freezer grade High-Density Polyethylene bucket/pail with tamper resistant lid.
Quantity
Total of 757 multiple sizes (6 fl oz cups, 16 fl oz cups, 32 fl oz cups and 1-gallon bucket/pail)
Reason
Soy Lecithin listed in ingredients statement, but Soy is not mentioned in the contains statement.
Recall initiation date
March 26, 2026
Report date
April 15, 2026
Classification date
Not published in this source record
Termination date
July 14, 2026
Distribution pattern
IL, IN and TX
UPC, lot, and code information
Lot Codes: 6 fl oz cups--- 00226, 03026, 05426, 33825 16 fl oz (or pint) -- 33825 1 gallon--05726
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 98651 with 2 other product entries in Public Health Trace.

FDA Recall United States Terminated 2026 recordClass II

Zarlengo Italian Ice

Product
Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon…
Published
April 15, 2026
Distribution
IL, IN and TX

View recall →

FDA Recall United States Terminated 2026 recordClass II

Zarlengo Italian Ice

Product
Zarlengo's Chocolate Chocolate Chip Gelato packaged in multi…
Published
April 15, 2026
Distribution
IL, IN and TX

View recall →

Responsible company: Zarlengo Italian Ice

Other recalls from Zarlengo Italian Ice

FDA Recall United States Terminated 2026 recordClass II

Zarlengo Italian Ice

Product
Zarlengo's Double Dark Chocolate Gelato packaged in 1 Gallon…
Published
April 15, 2026
Distribution
IL, IN and TX

View recall →

FDA Recall United States Terminated 2026 recordClass II

Zarlengo Italian Ice

Product
Zarlengo's Chocolate Chocolate Chip Gelato packaged in multi…
Published
April 15, 2026
Distribution
IL, IN and TX

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Illinois 1
Indiana 1
Texas 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.