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El Mirasol, Inc. Recall: Undeclared allergen: Wheat

United States

TerminatedClass II

Company
El Mirasol, Inc.
Product
Tortilla de Harina, 400 gr, 10 count, packaged in clear plas…
Recall date
April 29, 2024
Terminated
August 23, 2024
Source
FDA

Reason for recall

Undeclared allergen: Wheat

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Tortilla de Harina, 400 gr, 10 count, packaged in clear plastic bag, 20 packages per case. Not published in this source record 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 Lot #012324120800, Exp: 02/23/2024; Lot #021924120800, Exp: 03/19/2024.

Distribution

  • U.S. distribution within the state of Florida. No foreign distribution.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1375-2024
Event ID
94659
Status
Terminated
Classification
Class II
Company
El Mirasol, Inc.
Product description
Tortilla de Harina, 400 gr, 10 count, packaged in clear plastic bag, 20 packages per case.
Quantity
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
Undeclared allergen: Wheat
Recall initiation date
April 29, 2024
Report date
June 12, 2024
Classification date
Not published in this source record
Termination date
August 23, 2024
Distribution pattern
U.S. distribution within the state of Florida. No foreign distribution.
UPC, lot, and code information
Lot #012324120800, Exp: 02/23/2024; Lot #021924120800, Exp: 03/19/2024.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: El Mirasol, Inc.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.