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Lower risk Food recall · FDA · Published May 18, 2017

Dawn's Fresh Foods Tropical Fruit Dip Recall: Undeclared Yellow #5

Dawn's Fresh Foods recalls tropical fruit dip for undeclared yellow #5. Keep refrigerated for foodservice use only. Check production number 13638 for affected items.

🇺🇸 FDA recall #F-2397-2017FoodDawn's Fresh Foods ›
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Recalling firmMorski Brands, Inc. dba Dawn's Fresh Foods1530 La Dawn Dr · Portage, WI 53901-8823
✎ GovInfoNow plain-language explainer

What happened, in plain English

Dawn's Fresh Foods is recalling tropical fruit dip due to undeclared yellow #5. This artificial colorant poses a risk for people with allergies to this dye. The product is intended for foodservice use only and must be kept refrigerated. Read more at govinfonow.com/recall/21284-dawn-s-fresh-foods-tropical-fruit-dip-recall-undeclared-yellow.

Source Summary by GovInfoNow · govinfonow.com/recall/21284-dawn-s-fresh-foods-tropical-fruit-dip-recall-undeclared-yellow · Updated October 8, 2026 · FDA enforcement record: FDA #F-2397-2017

Cite this page

“Dawn's Fresh Foods Tropical Fruit Dip Recall: Undeclared Yellow #5.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21284-dawn-s-fresh-foods-tropical-fruit-dip-recall-undeclared-yellow. Based on FDA recall #F-2397-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2397-2017%22&limit=1).

Why it’s dangerous

The dip contains undeclared yellow #5, an artificial colorant that can cause allergic reactions in sensitive individuals. This is a food safety issue for people with specific allergies.

Who’s affected

Foodservice professionals and those handling the product in commercial kitchens. People with allergies to yellow #5 are at higher risk.

How to tell if you have this one

Check for the product name 'Dawn's Foods Tropical Fruit Dip' with weight 4 lbs (1.82Kg). Look for production number 13638 on the label.

  • Brand
    Dawn's Fresh Foods
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the production number 13638 on the label to confirm if it's affected.

Where it went and when

Where it was distributed

Distributed in Wisconsin.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: yesWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

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

States: Wisconsin.

Recall timeline

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

1. Firm started the recall: May 18, 201712. FDA classified it Class II: Jul 11, 201723. Published in FDA’s Enforcement Report: Jul 19, 201734. FDA terminated the recall: Sep 6, 201742017
  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-2397-2017 (May 18, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2397-2017 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