RecallHawk
Class II Recall

Bulk flour tortillas sold to food service. 20ct 6in flour. 12 packages of 20ct per case. Packed in clear plastic bag a

La Original Tortilla Co., Inc.

Summary

The FDA issued a Class II for Bulk flour tortillas sold to food service. 20ct 6in flour. 12 packages of 20ct by La Original Tortilla Co., Inc.. Reason: Undeclared ingredients including allergen Wheat.

Details

Source

Food Recall

External ID

F-1250-2024

Action Date

2024-05-29

Status

Terminated

Category

food

Product Description

Bulk flour tortillas sold to food service. 20ct 6in flour. 12 packages of 20ct per case. Packed in clear plastic bag and cardboard box.

Lot/Code Info: 1012

Quantity Affected: 35 cases

Reason for Recall

Undeclared ingredients including allergen Wheat

Distribution

Regional within in the state of Texas

Type: Voluntary: Firm initiated

Recall Initiated: 2024-04-16

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 27 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 (La Original Tortilla Co., Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does La Original Tortilla Co., Inc. have FDA actions?

This is the only FDA action we have on record for La Original Tortilla Co., Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1250-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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