Gerber Products Company dba Nestle Infant Nutrition Recall: Gerber Products Company is recalling Cheese Ravioli Gerber¿ Pasta Pick-Ups¿ because the egg allergen is missing from the "Contains" statement.

🇺🇸 United States

1. March 8, 2017 - Recall initiated
2. April 19, 2017 - Reported by source
3. February 14, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1922-2017

Event ID

76677

Status

Terminated

Classification

Class II

Company

Gerber Products Company dba Nestle Infant Nutrition

Product description

Gerber¿ Pasta Pick-Ups Cheese Ravioli Net Wt 6 oz (170g) Drained Wt 3 oz (85g) UPC 01500000907-6 , Truncated - written on package as: UPC 159070

Quantity

99,032 cases (8 units per case)

Reason

Gerber Products Company is recalling Cheese Ravioli Gerber¿ Pasta Pick-Ups¿ because the egg allergen is missing from the "Contains" statement.

Recall initiation date

March 8, 2017

Report date

April 19, 2017

Classification date

Not published in this source record

Termination date

February 14, 2018

Distribution pattern

Nationwide

UPC, lot, and code information

UPC 01500000907-6; All codes

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

July 18, 2026 ET

Responsible company: Gerber Products Company dba Nestle Infant Nutrition

Other recalls from Gerber Products Company dba Nestle Infant Nutrition

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.

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.

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