Tortilla de Harina, 400 gr, 10 count, packaged in clear plastic bag, 20 packages per case.
Summary
The FDA issued a Class II for Tortilla de Harina, 400 gr, 10 count, packaged in clear plastic bag, 20 packages by El Mirasol, Inc.. Reason: Undeclared allergen: Wheat.
Details
Source
Food Recall
External ID
F-1375-2024
Action Date
2024-06-12
Status
Terminated
Category
food
Product Description
Tortilla de Harina, 400 gr, 10 count, packaged in clear plastic bag, 20 packages per case.
Lot/Code Info: Lot #012324120800, Exp: 02/23/2024; Lot #021924120800, Exp: 03/19/2024.
Quantity Affected: 50 cases of 20 packages of 10 tortillas, Lot #012324120800, Exp: 02/23/2024; 50 cases of 20 packages of 10 tortillas, Lot #021924120800, Exp: 03/19/24
Reason for Recall
Undeclared allergen: Wheat
Distribution
U.S. distribution within the state of Florida. No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-04-29
Company
Plant City, FL
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 77 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 (El Mirasol, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does El Mirasol, Inc. have FDA actions?
This is the only FDA action we have on record for El Mirasol, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1375-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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