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Lower risk Food recall · FDA · Published May 25, 2017

California Sun Dry Foods Sun Dried Tomato Pesto Recall: Incorrect Allergen Labeling

California Sun Dry Foods recalls Sun Dried Tomato Pesto jars with incorrect allergen labeling. The product may contain undeclared almonds and milk. Consumers should check labels and contact the company for details.

🇺🇸 FDA recall #F-2319-2017FoodCalifornia Sun Dry Foods ›
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Contact the company

Recalling firmCalifornia Sun Dry Foods169 Front St Ste 100 · Danville, CA 94526-3321
✎ GovInfoNow plain-language explainer

What happened, in plain English

California Sun Dry Foods is recalling Sun Dried Tomato Pesto jars because the label incorrectly lists ingredients without declaring almonds and milk. This poses a risk for people with allergies to these ingredients, as they might unknowingly consume them. Read more at govinfonow.com/recall/21158-california-sun-dry-foods-sun-dried-tomato-pesto-recall-incorrect.

Source Summary by GovInfoNow · govinfonow.com/recall/21158-california-sun-dry-foods-sun-dried-tomato-pesto-recall-incorrect · Updated October 8, 2026 · FDA enforcement record: FDA #F-2319-2017

Cite this page

“California Sun Dry Foods Sun Dried Tomato Pesto Recall: Incorrect Allergen Labeling.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21158-california-sun-dry-foods-sun-dried-tomato-pesto-recall-incorrect. Based on FDA recall #F-2319-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2319-2017%22&limit=1).

Why it’s dangerous

The product label incorrectly lists ingredients without declaring almonds and milk. This means people with allergies to these ingredients could unknowingly consume them and experience allergic reactions.

Who’s affected

People with almond or milk allergies who consume the product may be at risk. The recall affects consumers who bought the specific jar size and model with incorrect labeling.

How to tell if you have this one

Check for jars labeled 'California Sun Dry Sun Dried Tomato Pesto' with a net weight of 8.5 oz (241g) and a glass container. The product was sold with incorrect allergen labeling.

  • Brand
    California Sun Dry Foods
  • Product
    California Sun Dry Sun Dried Tomato Pesto; NET WT. 8.5 oz. (241g) glass jar; Ingredients (incorrect) Garlic, Canola
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Label for Allergens

    Look for the label that lists 'Garlic, Canola' as ingredients without mentioning almonds or milk.

Where it went and when

Where it was distributed

Distributed in 23 states.

Alaska: not listedAKMaine: yesMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: not listedNEMissouri: yesMOKentucky: yesKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: yesKSArkansas: not listedARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “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.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Colorado, Georgia, Indiana, Kansas, Kentucky, Maine, Maryland, Massachusetts, Missouri, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin.

Recall timeline

FDA terminated this recall 4 months after the firm started it.

1. Firm started the recall: May 25, 201712. FDA classified it Class I: Jun 2, 201723. Published in FDA’s Enforcement Report: Jun 14, 201734. FDA terminated the recall: Sep 11, 201742017
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-2319-2017 (May 25, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2319-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA