RecallHawk
Class II Recall

Panaderia Guatemex - Sheca Redonda packaged in plastic bag

Panaderia Guatemex

Summary

The FDA issued a Class II for Panaderia Guatemex - Sheca Redonda packaged in plastic bag by Panaderia Guatemex. Reason: Undeclared Allergen - Soy.

Details

Source

Food Recall

External ID

F-1713-2024

Action Date

2024-08-14

Status

Terminated

Category

food

Product Description

Panaderia Guatemex - Sheca Redonda packaged in plastic bag

Lot/Code Info: Best By 07/21/2024 No other code information

Quantity Affected: 170 bags

Reason for Recall

Undeclared Allergen - Soy

Distribution

GA, KY, TN

Type: Voluntary: Firm initiated

Recall Initiated: 2024-07-02

Company

Panaderia Guatemex

Cookeville, TN

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

Panaderia Guatemex has 15 FDA actions in our database, including 15 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 (Panaderia Guatemex) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Panaderia Guatemex have FDA actions?

Panaderia Guatemex has 15 FDA actions in our database, including 15 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1713-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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