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Fanega Mexican Food Products, Inc. Recall: Fanega Mexican Foods is recalling flour tortillas because they contain undeclared wheat.

United States

TerminatedClass II

Company
Fanega Mexican Food Products, Inc.
Product
10" Flour Tortillas 12 count, Net Wt. 25oz (732g)
Recall date
October 26, 2016
Terminated
November 10, 2016
Source
FDA

Reason for recall

Fanega Mexican Foods is recalling flour tortillas because they contain undeclared wheat.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
10" Flour Tortillas 12 count, Net Wt. 25oz (732g) Not published in this source record 280 units 10-28-16 10-29-16 10-30-16 11-1-16 11-2-16 11-4-16 11-5-16

Distribution

  • AZ

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0311-2017
Event ID
75549
Status
Terminated
Classification
Class II
Company
Fanega Mexican Food Products, Inc.
Product description
10" Flour Tortillas 12 count, Net Wt. 25oz (732g)
Quantity
280 units
Reason
Fanega Mexican Foods is recalling flour tortillas because they contain undeclared wheat.
Recall initiation date
October 26, 2016
Report date
November 9, 2016
Classification date
Not published in this source record
Termination date
November 10, 2016
Distribution pattern
AZ
UPC, lot, and code information
10-28-16 10-29-16 10-30-16 11-1-16 11-2-16 11-4-16 11-5-16
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Fanega Mexican Food Products, Inc.

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Arizona 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

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.