Seggiano Artichoke Sauce Mislabelled with Cashews - Recall
Seggiano Artichoke & Garlic Sauce & Spread (200g) was mislabeled as不含 cashews, containing undeclared cashews. Consumers should check UPC 812603020381.
Lower-risk recall
The Tuscan Kale Pesto was mislabeled as Seggiano Artichoke & Garlic Sauce & Spread and therefore, contains undeclared cashews.
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What happened, in plain English
Seggiano Artichoke & Garlic Sauce & Spread (200g) was recalled because it was mislabeled as not containing cashews when it actually does. This could cause allergic reactions for people sensitive to cashews. Read more at govinfonow.com/recall/19655-seggiano-artichoke-sauce-mislabelled-with-cashews-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/19655-seggiano-artichoke-sauce-mislabelled-with-cashews-recall · Updated October 7, 2026 · FDA enforcement record: FDA #F-0923-2018
Cite this page
“Seggiano Artichoke Sauce Mislabelled with Cashews - Recall.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19655-seggiano-artichoke-sauce-mislabelled-with-cashews-recall. Based on FDA recall #F-0923-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0923-2018%22&limit=1).
Why it’s dangerous
The sauce was mislabeled as cashew-free but contains cashews. This means people with cashew allergies could have an allergic reaction if they consume it.
Who’s affected
People who own or use this sauce are affected, especially those with cashew allergies. The recall covers specific packaging with UPC 812603020381.
How to tell if you have this one
Check for the glass jar labeled 'Seggiano Artichoke & Garlic Sauce & Spread' with UPC 812603020381. The batch number is 326 - 17/3 and best by date is 05/2019.
- Brand
Seggiano- Product
Seggiano Artichoke & Garlic Sauce & Spread Net Weight 200g, 7.1 oz, packaged in Glass jar, UPC Code: 812603020381- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 812603020381 on the glass jar packaging.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 32 states.
FDA distribution: “Distributed nationwide to States: NY, CT, NJ, MN, VT, NH, MA, PA, OH, VA, MD, WV, KY, DC, FL, MT, ID, WY, UT, CO, KS, NM, HI, AZ, NV, ND, SD, MN, WI, MI, IN, IL, IA, MS, NB No foreign or govt/VA/military consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arizona, Colorado, Connecticut, District of Columbia, Florida, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Montana, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Dakota, Ohio, Pennsylvania, South Dakota, Utah, Vermont, Virginia, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA terminated this recall 2.3 years after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class I
- 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-0923-2018 (February 15, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0923-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.