La Torre Foods Usa, Inc. Recall: Calcium caseinate is declared on the label, but milk is not listed.

United States

TerminatedClass II

Company: La Torre Foods Usa, Inc.
Product: la Torre Copito Marshmallow Chocolate Cookie NET WT 4.94 oz…
Recall date: July 26, 2016
Terminated: May 11, 2017
Source: FDA

Reason for recall

Calcium caseinate is declared on the label, but milk is not listed.

July 26, 2016 - Recall initiated
August 31, 2016 - Reported by source
May 11, 2017 - Recall terminated

Recalled products
Product description	UPC	Quantity	Lot / code information
la Torre Copito Marshmallow Chocolate Cookie NET WT 4.94 oz packaged in a cardboard box.	Not published in this source record	Not published in this source record	Not published in this source record

Distribution

Nationwide throughout the US.

Official source record

Agency: FDA
Dataset: FDA Food Enforcement (Recalls)
Recall number: F-1973-2016
Status: Terminated
Classification: Class II
Company: La Torre Foods Usa, Inc.
Product description: la Torre Copito Marshmallow Chocolate Cookie NET WT 4.94 oz packaged in a cardboard box.
Quantity: Not published in this source record
Reason: Calcium caseinate is declared on the label, but milk is not listed.
Recall initiation date: July 26, 2016
Report date: August 31, 2016
Classification date: Not published in this source record
Termination date: May 11, 2017
Distribution pattern: Nationwide throughout the US.
UPC, lot, and code information: Not published in this source record
Voluntary or mandated: Not published in this source record
Initial notification method: Not published in this source record
Source last updated: Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date: July 18, 2026 ET

Responsible company: La Torre Foods Usa, Inc.

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: July 18, 2026 ET

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.

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