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Lower risk Food recall · FDA · Published March 4, 2026

Disaron: Montebianco Vegan Bag Recall - Undeclared Milk Allergen Risk

Disaronno recalls Montebianco 113542 Base Vegan bags due to undeclared milk allergen exceeding safe levels despite label warning. Consumers should check lot numbers and contact for refunds.

🇺🇸 FDA recall #H-0690-2026FoodDisaronno ›
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Contact the company

Recalling firmDisaronno Ingredients S.p.a.Via Quattro Novembre 12 · Altavilla Vicentina, Italy
✎ GovInfoNow plain-language explainer

Disaronno is recalling Montebianco 113542 Base Vegan bags because they contain milk allergen levels above safe limits, even though the product labels say 'may contain milk.' This poses a risk for people with milk allergies. Read more at govinfonow.com/recall/6672-disaron-montebianco-vegan-bag-recall-undeclared-milk-allergen-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/6672-disaron-montebianco-vegan-bag-recall-undeclared-milk-allergen-risk · Updated August 17, 2026 · Official notice: FDA #H-0690-2026

Cite this page

“Disaron: Montebianco Vegan Bag Recall - Undeclared Milk Allergen Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6672-disaron-montebianco-vegan-bag-recall-undeclared-milk-allergen-risk. Based on FDA recall #H-0690-2026.

The FDA announced on March 4, 2026, that Disaronno Ingredients S.p.a. is recalling Montebianco Base Vegan bags due to undeclared milk allergens that exceed acceptable levels. The agency issued recall number H-0690-2026 for the Class II voluntary recall.

How to tell if you have it

  • Brand: Disaronno
  • Product: Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag
  • Lot#: L070725 0727
  • BBE: 31.07.2027
  • Distribution: MD

The hazard

The product contains undeclared milk allergens that exceed acceptable levels, despite the label stating May contain milk. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include Frankie's Vegan Cheddar Puffs Recalled for Undeclared Milk (2026-08-05), D'Dioses Tamarindo Ice Pop Recall: Undeclared Allergens (2026-05-04), and Marquez Brothers Horchata Powder Recall: Undeclared Milk Hazard (2026-04-07).

How to tell if you have this one

Check for lot number L070725 0727 on the bag. The product was sold in 2 kg bags, 8 per master case, with a total case weight of 16 kg.

  • Brand
    Disaronno
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for lot number L070725 0727 on the bag to confirm if it's recalled.

Where it went and when

Where it was distributed

Distributed in Maryland.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: 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: yesMDDelaware: 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: “Product distributed in MD” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maryland.

Recall timeline

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

1. Firm started the recall: Mar 4, 202612. FDA classified it Class II: May 4, 202623. Published in FDA’s Enforcement Report: May 13, 202634. FDA terminated the recall: Jun 24, 202642026
  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 #H-0690-2026 (March 4, 2026)
  • Plain-language summary written by qwen3:4b on August 17, 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