Class IITerminated in FDA datasetRecall initiated Dec 7, 2017

Single-serve plastic pack: Newman's Own Lite Sesame Ginger; Net Wt. 1.5 OZ.; Produced…

Recalling firm: Ventura Foods, LLC

Why it was recalled

A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jun 28, 2018.

Check your package

Compare the exact product and package details with the label you have.

ProductSingle-serve plastic pack: Newman's Own Lite Sesame Ginger; Net Wt. 1.5 OZ.; Produced exclusively for Newman's Own, Inc., Westport CT 06880 Carton: Newman's Own, Inc., Westport CT 06880; 100/1.5 OZ; Lite Sesame Ginger, code: 042918
Package size1.5 OZ

FDA code information

Code: 042918; lot date 4/29/2018

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Single-serve plastic pack: Newman's Own Lite Sesame Ginger; Net Wt. 1.5 OZ.; Produced exclusively for Newman's Own, Inc., Westport CT 06880 Carton: Newman's Own, Inc., Westport CT 06880; 100/1.5 OZ; Lite Sesame Ginger, code: 042918

Original FDA recall reason

A plastic foreign object was inadvertently introduced into the product stream. The firm is recalling product as not all plastic has been accounted.

Recall details

Recall number
F-0599-2018
Event ID
78713
FDA status
Terminated
Initiated
Dec 7, 2017
Reported
Jan 24, 2018
Classified
Jan 19, 2018
Terminated
Jun 28, 2018
Quantity
38 cases
Location
Chambersburg, PA, 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

Nationwide

FDA source record · F-0599-2018

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

Follow official FDA and manufacturer guidance.