Roasted Red Pepper 12" Supreme Flour Wraps, Tortilleria Sonora, Inc.
Summary
The FDA issued a Class II for Roasted Red Pepper 12" Supreme Flour Wraps, Tortilleria Sonora, Inc. by Tortilleria Sonora. Reason: Flour tortillas list "Bleached enriched flour" on the case label but do not mention the presence of wheat. Therefore the product contains undeclared w.
Details
Source
Food Recall
External ID
F-0981-2021
Action Date
2021-09-22
Status
Terminated
Category
food
Product Description
Roasted Red Pepper 12" Supreme Flour Wraps, Tortilleria Sonora, Inc.
Lot/Code Info: 8/25
Quantity Affected: 1 case
Reason for Recall
Flour tortillas list "Bleached enriched flour" on the case label but do not mention the presence of wheat. Therefore the product contains undeclared wheat.
Distribution
Distributed to one restaurant in Iowa.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-08-25
Company
Des Moines, IA
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 30 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 (Tortilleria Sonora) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tortilleria Sonora have FDA actions?
This is the only FDA action we have on record for Tortilleria Sonora in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0981-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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