RecallHawk
Class I Recall

Velvet Ice Cream Raspberry Fudge Cordial 1.75 quarts (56oz) 6 quarts per case

Velvet Ice Cream Company

Summary

The FDA issued a Class I for Velvet Ice Cream Raspberry Fudge Cordial 1.75 quarts (56oz) 6 quarts per cas by Velvet Ice Cream Company. Reason: Undeclared Allergen.

Details

Source

Food Recall

External ID

F-1017-2021

Action Date

2021-10-06

Status

Terminated

Category

food

Product Description

Velvet Ice Cream Raspberry Fudge Cordial 1.75 quarts (56oz) 6 quarts per case

Lot/Code Info: UPC 070682100497 Julian Date 19521 Lot Code A2195211424600019926012

Quantity Affected: 11988 units

Reason for Recall

Undeclared Allergen

Distribution

Indiana, Kentucky, Michigan, Ohio, West Virginia

Type: Voluntary: Firm initiated

Recall Initiated: 2021-09-06

Company

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 43 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (Velvet Ice Cream Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Velvet Ice Cream Company have FDA actions?

This is the only FDA action we have on record for Velvet Ice Cream Company in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1017-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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