RecallHawk
Class II Recall

Danncy Vainilla Pure Mexican Vanilla Extract Clear Gluten Free Produced by Juan Miguel Anzaldua Gutierrez NET 33.8 FL OZ

Danncy Vainilla

Summary

The FDA issued a Class II for Danncy Vainilla Pure Mexican Vanilla Extract Clear Gluten Free Produced by Juan by Danncy Vainilla. Reason: The firm's vanilla product contains coumarin, a prohibited substance..

Details

Source

Food Recall

External ID

F-0688-2023

Action Date

2023-04-05

Status

Terminated

Category

food

Product Description

Danncy Vainilla Pure Mexican Vanilla Extract Clear Gluten Free Produced by Juan Miguel Anzaldua Gutierrez NET 33.8 FL OZ (1.0L) UPC 7503000781137 packaged in clear plastic bottles and Danncy Vainilla Pure Mexican Vanilla Extract Gluten Free Produced by Juan Miguel Anzaldua Gutierrez NET 33.8 FL OZ (1.0L) UPC 7503000781106 packaged in clear plastic bottles

Lot/Code Info: All Danncy Vanilla Products

Quantity Affected: ~1,542 boxes

Reason for Recall

The firm's vanilla product contains coumarin, a prohibited substance.

Distribution

Texas and California

Type: Voluntary: Firm initiated

Recall Initiated: 2023-02-05

Company

Danncy Vainilla

Laredo, TX

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

How often does Danncy Vainilla have FDA actions?

This is the only FDA action we have on record for Danncy Vainilla in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0688-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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