Class ITerminated in FDA datasetRecall initiated May 25, 2017

California Sun Dry Sun Dried Tomato Pesto; NET WT. 8.5 oz. (241g) glass jar

Recalling firm: California Sun Dry Foods

Why it was recalled

Firm employee noticed that incorrect back label was attached to Sun-Dried Tomato Pesto and therefore did not declare the allergens of almonds and milk..

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: Sep 11, 2017.

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ProductCalifornia Sun Dry Sun Dried Tomato Pesto; NET WT. 8.5 oz. (241g) glass jar; Ingredients (incorrect) Garlic, Canola oil, sundried tomatoes (preserved with sulfating agents) water, sola oil, spices, onion, salt, citric acid,, soy lecithin. Partially processed with Genetic Engineering. UPC 7 38203 10911 3 California Sun Dry Foods, Danville, California. Product of the USA.
Package size8.5 oz
UPC738203109113

FDA code information

PTP0567A Use by 25 FEB2019.

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Full FDA record and distribution details

Original product description

California Sun Dry Sun Dried Tomato Pesto; NET WT. 8.5 oz. (241g) glass jar; Ingredients (incorrect) Garlic, Canola oil, sundried tomatoes (preserved with sulfating agents) water, sola oil, spices, onion, salt, citric acid,, soy lecithin. Partially processed with Genetic Engineering. UPC 7 38203 10911 3 California Sun Dry Foods, Danville, California. Product of the USA.

Extracted codes and context

TypeCode / valueContext
UPC738203109113itric acid,, soy lecithin. Partially processed with Genetic Engineering. UPC 7 38203 10911 3 California Sun Dry Foods, Danville, California. Product of the USA.

Original FDA recall reason

Firm employee noticed that incorrect back label was attached to Sun-Dried Tomato Pesto and therefore did not declare the allergens of almonds and milk..

Recall details

Recall number
F-2319-2017
Event ID
77376
FDA status
Terminated
Initiated
May 25, 2017
Reported
Jun 14, 2017
Classified
Jun 2, 2017
Terminated
Sep 11, 2017
Quantity
2868 cases (6 jars per case of 17,208 individual units)
Location
Danville, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

US distribution only. KS, MD, PA, CA, WA, MO, NC, SC, ME, NY, CO, OH, KY, TN, VA, IN, GA, OR, AZ,UT, WI, TX, MA.

FDA source record · F-2319-2017

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

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