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Lower risk Food recall · FDA · Published April 5, 2018

Cut Fruit Express Bruschetta Mix Recalled for Undeclared Milk & Soy

Cut Fruit Express recalls Bruschetta Mix products containing undeclared milk and soy. Consumers should check product labels for specific brands and UPC codes to avoid potential allergic reactions.

🇺🇸 FDA recall #F-1106-2018FoodCut Fruit Express ›
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Contact the company

Recalling firmCut Fruit Express, Inc.11585 Courthouse Blvd · Inver Grove Heights, MN 55077-5911
✎ GovInfoNow plain-language explainer

What happened, in plain English

Cut Fruit Express is recalling Bruschetta Mix products that contain undeclared milk and soy. This poses a risk for people with milk or soy allergies who may experience allergic reactions if they consume these products. Read more at govinfonow.com/recall/19267-cut-fruit-express-bruschetta-mix-recalled-for-undeclared-milk-soy.

Source Summary by GovInfoNow · govinfonow.com/recall/19267-cut-fruit-express-bruschetta-mix-recalled-for-undeclared-milk-soy · Updated October 7, 2026 · FDA enforcement record: FDA #F-1106-2018

Cite this page

“Cut Fruit Express Bruschetta Mix Recalled for Undeclared Milk & Soy.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19267-cut-fruit-express-bruschetta-mix-recalled-for-undeclared-milk-soy. Based on FDA recall #F-1106-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1106-2018%22&limit=1).

Why it’s dangerous

The Bruschetta Mix products contain undeclared milk and soy, which can cause allergic reactions in sensitive individuals. This is a food safety issue related to ingredient labeling.

Who’s affected

People with milk or soy allergies are at risk of allergic reactions if they consume the recalled Bruschetta Mix products. The recall affects specific brands and sizes sold between April 5 and April 12, 2018.

How to tell if you have this one

Check for the following brands and sizes: Tastebuds (12 oz. UPC 38232-37403), Quick & Easy Fresh Cut (12 oz. UPC 38232-37403), H. Brooks (5#), Reinhart (Brushetta Mix 5#), and Upper Lakes Foods (Bruschetta Mix 5#). Products were distributed between April 5 and April 12, 2018.

  • Brand
    Cut Fruit Express
  • Product
    Bruschetta Mix packaged under the following brands and sizes: 1. Tastebuds, Net Wt. 12 oz. (340g), UPC 38232-37403
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Labels

    Look for the brand name and UPC code on the product label to determine if it matches the recalled items.

Where it went and when

Where it was distributed

Distributed in Minnesota.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: not listedILWisconsin: not listedWIMichigan: 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: “MN” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Minnesota.

Recall timeline

FDA terminated this recall 15 months after the firm started it.

1. Firm started the recall: Apr 5, 201812. FDA classified it Class I: Apr 17, 201823. Published in FDA’s Enforcement Report: Apr 18, 201834. FDA terminated the recall: Jun 27, 2019420182019
  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-1106-2018 (April 5, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1106-2018 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