Class II Recall

Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag, packed 8 bags per master case of 2 Kg (4.41 lb) each total case weig

Summary

The FDA issued a Class II for Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag, packed 8 bags per master cas by Disaronno Ingredients S.p.a.. Reason: Undeclared allergen Milk. The presence of the milk allergen in the product was found to exceed acceptable levels despite the product being labeled wit.

Details

Source

Food Recall

External ID

H-0690-2026

Action Date

2026-05-13

Status

Terminated

Product Description

Montebianco, 113542 Base Vegan, 2 Kg (4.41 Lb) Bag, packed 8 bags per master case of 2 Kg (4.41 lb) each total case weight,16 Kg / 35.27 lb

Lot/Code Info: Lot#L070725 0727 BBE: 31.07.2027

Quantity Affected: 15 boxes (8 bags per case of 2Kg 4,41 lb each one) and 6 bags

Reason for Recall

Undeclared allergen Milk. The presence of the milk allergen in the product was found to exceed acceptable levels despite the product being labeled with the statement *May contain milk. *

Distribution

Product distributed in MD

Type: Voluntary: Firm initiated

Recall Initiated: 2026-03-04

Company

Disaronno Ingredients S.p.a.

Altavilla Vicentina

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 93 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Disaronno Ingredients S.p.a.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Disaronno Ingredients S.p.a. have FDA actions?

This is the only FDA action we have on record for Disaronno Ingredients S.p.a. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0690-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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