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Lower risk Food recall · FDA · Published November 9, 2017

Figi's Dark Chocolate Gingersnaps Recall: Undeclared Milk Hazard

Figi's recalls Dark Chocolate Gingersnaps with undeclared milk. Consumers should check packaging for product codes 038-6025-901 or #0368 Christmas Ginger Snap Variety.

🇺🇸 FDA recall #F-0518-2018FoodFigi's ›
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Recalling firmFigi's, Inc3200 S Central Ave · Marshfield, WI 54404-0001
✎ GovInfoNow plain-language explainer

What happened, in plain English

Figi's is recalling Dark Chocolate covered Gingersnaps that contain undeclared milk. This poses a risk for people with milk allergies who may experience allergic reactions. The recall affects specific packaging sizes and product codes. Read more at govinfonow.com/recall/20051-figi-s-dark-chocolate-gingersnaps-recall-undeclared-milk-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/20051-figi-s-dark-chocolate-gingersnaps-recall-undeclared-milk-hazard · Updated October 7, 2026 · FDA enforcement record: FDA #F-0518-2018

Cite this page

“Figi's Dark Chocolate Gingersnaps Recall: Undeclared Milk Hazard.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20051-figi-s-dark-chocolate-gingersnaps-recall-undeclared-milk-hazard. Based on FDA recall #F-0518-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0518-2018%22&limit=1).

Why it’s dangerous

The gingersnaps contain undeclared milk, meaning they may trigger allergic reactions in individuals with milk allergies. This is a food safety issue that requires consumers to check for milk content before consumption.

Who’s affected

People with milk allergies are at risk of allergic reactions from these gingersnaps. The recall applies to specific product codes and packaging sizes.

How to tell if you have this one

Check for product code 038-6025-901 on clear plastic ziplock bags or product #0368 Christmas Ginger Snap Variety in decorative circular gift tins. The packaging sizes range from 8 oz to 12 oz.

  • Brand
    Figi's
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Packaging

    Look for product code 038-6025-901 on clear plastic ziplock bags or product #0368 Christmas Ginger Snap Variety in decorative circular gift tins.

Where it went and when

Where it was distributed

Distributed nationwide; the notice names 17 states.

Alaska: nationwideAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: nationwideNHWashington: named in the noticeWAIdaho: nationwideIDMontana: nationwideMTNorth Dakota: nationwideNDMinnesota: nationwideMNIllinois: named in the noticeILWisconsin: nationwideWIMichigan: nationwideMINew York: named in the noticeNYRhode Island: nationwideRIMassachusetts: nationwideMAOregon: nationwideORNevada: named in the noticeNVWyoming: nationwideWYSouth Dakota: nationwideSDIowa: named in the noticeIAIndiana: nationwideINOhio: named in the noticeOHPennsylvania: nationwidePANew Jersey: nationwideNJConnecticut: nationwideCTCalifornia: named in the noticeCAUtah: nationwideUTColorado: nationwideCONebraska: nationwideNEMissouri: named in the noticeMOKentucky: named in the noticeKYWest Virginia: nationwideWVVirginia: nationwideVAMaryland: named in the noticeMDDelaware: nationwideDEArizona: nationwideAZNew Mexico: nationwideNMKansas: nationwideKSArkansas: named in the noticeARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: nationwideDCOklahoma: nationwideOKLouisiana: nationwideLAMississippi: nationwideMSAlabama: nationwideALGeorgia: named in the noticeGAHawaii: nationwideHITexas: named in the noticeTXFlorida: named in the noticeFL

FDA distribution: “Nationwide thru mail orders to include: AR, CA, FL, GA, IA, IL, KY, MD, MO, NC, NV, NY, OH, SC, TN, TX, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Arkansas, California, Florida, Georgia, Illinois, Iowa, Kentucky, Maryland, Missouri, Nevada, New York, North Carolina, Ohio, South Carolina, Tennessee, Texas, Washington.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Nov 9, 201712. FDA classified it Class II: Dec 31, 201723. Published in FDA’s Enforcement Report: Jan 10, 201834. FDA terminated the recall: Oct 2, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class II
  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-0518-2018 (November 9, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0518-2018 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.
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