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Ruiz Food Products Inc Recall: Firm received two complaints of foreign object in frozen burrito product.

United States

TerminatedClass II

Company
Ruiz Food Products Inc
Product
El Monterey XXL Bean and Cheese Burrito; 9.5 oz. frozen bur…
Recall date
August 28, 2019
Terminated
January 21, 2020
Source
FDA

Reason for recall

Firm received two complaints of foreign object in frozen burrito product.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
El Monterey XXL Bean and Cheese Burrito; 9.5 oz. frozen burrito in film Microwaveable Case UPC: UPC 1 00 71007 06217 6; Sell unit UPC: 0 71007 06217 9 Not published in this source record 301 cases - 42 burritos per case res#06217, Lot#19133:

Distribution

  • CT
  • MN
  • OR
  • SC

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2150-2019
Event ID
83663
Status
Terminated
Classification
Class II
Company
Ruiz Food Products Inc
Product description
El Monterey XXL Bean and Cheese Burrito; 9.5 oz. frozen burrito in film Microwaveable Case UPC: UPC 1 00 71007 06217 6; Sell unit UPC: 0 71007 06217 9
Quantity
301 cases - 42 burritos per case
Reason
Firm received two complaints of foreign object in frozen burrito product.
Recall initiation date
August 28, 2019
Report date
September 18, 2019
Classification date
Not published in this source record
Termination date
January 21, 2020
Distribution pattern
CT, MN, OR, SC
UPC, lot, and code information
res#06217, Lot#19133:
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Ruiz 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
Connecticut 1
Minnesota 1
Oregon 1
South Carolina 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.