RecallHawk
Class II Recall

Vitony Bakery, Bizcocho de Queso (cheesecake), PESO NETO 14oz (397g) (12 (14 oz) packages per case)

Vitony Bakery, Inc.

Summary

The FDA issued a Class II for Vitony Bakery, Bizcocho de Queso (cheesecake), PESO NETO 14oz (397g) (12 (14 oz) by Vitony Bakery, Inc.. Reason: Undeclared allergens FD&C Yellow #5, Yellow #6.

Details

Source

Food Recall

External ID

F-1061-2024

Action Date

2024-03-20

Status

Terminated

Category

food

Product Description

Vitony Bakery, Bizcocho de Queso (cheesecake), PESO NETO 14oz (397g) (12 (14 oz) packages per case)

Lot/Code Info: None in product label

Quantity Affected: 6,916 units

Reason for Recall

Undeclared allergens FD&C Yellow #5, Yellow #6

Distribution

Domestic consignee's only (Puerto Rico PR)

Type: Voluntary: Firm initiated

Recall Initiated: 2024-02-29

Company

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

Vitony Bakery, Inc. has 2 FDA actions in our database, including 2 recalls.

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

How often does Vitony Bakery, Inc. have FDA actions?

Vitony Bakery, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1061-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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