RecallHawk
Class I Recall

Belgian Yummies Homemade Ice Cream Horchata Gelato. Packaged in 4.75 Liter gray pan.

Belgian Yummies

Summary

The FDA issued a Class I for Belgian Yummies Homemade Ice Cream Horchata Gelato. Packaged in 4.75 Liter gray by Belgian Yummies. Reason: Undeclared Allergen: milk and wheat..

Details

Source

Food Recall

External ID

F-1236-2024

Action Date

2024-05-15

Status

Terminated

Category

food

Product Description

Belgian Yummies Homemade Ice Cream Horchata Gelato. Packaged in 4.75 Liter gray pan.

Lot/Code Info: No lot numbers provided; Expiration date is 6 months from production date.

Quantity Affected: 12

Reason for Recall

Undeclared Allergen: milk and wheat.

Distribution

The products were only distributed in the state of Florida.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-20

Company

Belgian Yummies

Fort Myers, FL

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Belgian Yummies has 9 FDA actions in our database, including 9 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Belgian Yummies) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Belgian Yummies have FDA actions?

Belgian Yummies has 9 FDA actions in our database, including 9 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1236-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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