Class IIITerminated in FDA datasetJul 25, 2018

Severino Home Made, Artisanal Small Batch Pasta, Raviolini Cheese, 9 units x 9 oz per case. Expiration March 2019.

Recalling firm: Severino Pasta Manufacturing, Inc.

Why it was recalled

Severino Pasta Manufacturing, Inc. has initiated a recall of their Severino Pasta Super Fresh Cheese Raviolini due to undeclared eggs. The retail unit has the correct label on top, Cheese Raviolini which declares the precense of eggs in the ingredient statement and contains statement. However, the product has the incorrect label on the bottom, Cheese Rigatoni, which does not declare eggs in the ingredient statement or contains statement. The Raviolini label declares: Wheat, Milk, and Eggs whereas the Rigatoni label declares: Wheat and Milk. Since both labels are on the product consumers may be confused as to which ingredients are actually present.

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The exact product

Severino Home Made, Artisanal Small Batch Pasta, Raviolini Cheese, 9 units x 9 oz per case. Expiration March 2019.

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

No specific lot or batch information was provided in this FDA record.

Recall details

Recall number
F-1823-2018
Event ID
80677
FDA status
Terminated
Initiated
Jul 25, 2018
Reported
Aug 22, 2018
Classified
Aug 14, 2018
Terminated
Oct 14, 2021
Quantity
42 cases, 378 units were produced
Location
Westmont, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Product was distributed to Whole Foods Markets in the Florida and the NE/NA Region (Massachusetts, Connecticut, Rhode Island, New Hampshire, Maine) Whole Foods Florida DC, 2700 NW 19th Street, Ste 100, Pompano Beach, FL. Whole Foods NE/NA DC, 400 East Johnson Ave, Cheshire, CT. 06410

FDA source record · F-1823-2018

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.