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Class IIITerminated in FDA datasetRecall initiated Oct 13, 2017

White Polenta, San Gennaro brand, 12/16oz packages

Recalling firm: San Gennaro Foods, Inc

Why it was recalled

Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food…

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: May 18, 2018.

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

ProductWhite Polenta, San Gennaro brand, 12/16oz packages, UPC# 7-62676-17400-2 White Polenta, San Gennaro brand, 6/16oz packages UPC# 7-62676-17400-2 Ingredients: Water, White Corn Meal, Salt, Tartaric Acid
Package size16oz
UPC762676174002

FDA code information

030618, 050818

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

Full FDA record and distribution details

Original product description

White Polenta, San Gennaro brand, 12/16oz packages, UPC# 7-62676-17400-2 White Polenta, San Gennaro brand, 6/16oz packages UPC# 7-62676-17400-2 Ingredients: Water, White Corn Meal, Salt, Tartaric Acid

Extracted codes and context

TypeCode / valueContext
UPC762676174002White Polenta, San Gennaro brand, 12/16oz packages, UPC# 7-62676-17400-2 White Polenta, San Gennaro brand, 6/16oz packages UPC# 7-62676-17400-2 Ingredients: Water, White Corn Meal, Salt
UPC762676174002 UPC# 7-62676-17400-2 White Polenta, San Gennaro brand, 6/16oz packages UPC# 7-62676-17400-2 Ingredients: Water, White Corn Meal, Salt, Tartaric Acid

Original FDA recall reason

Date coding ink was being printed directly on the food contact surface of packaging, allowing the ink to be in direct contact with the product. The ink is not approved for food use.

Recall details

Recall number
F-0126-2018
Event ID
78290
FDA status
Terminated
Initiated
Oct 13, 2017
Reported
Nov 15, 2017
Classified
Nov 8, 2017
Terminated
May 18, 2018
Quantity
285 cases
Location
Kent, WA, 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

CA, CO, FL, GA, IL, IN, MD, ME, MI, NJ, NY, OR, PA, SC, TX, VA, WA, WI and Canada.

FDA source record · F-0126-2018

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

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