Class ITerminated in FDA datasetRecall initiated Jan 11, 2019

El Guapo Pasilla-Ancho Chile Pods 2oz, 7.5oz, 11oz

Recalling firm: McCormick & Company, Inc. - Flavor Manufacturing Center

Why it was recalled

Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary recall of El Guapo Chile Habanero and Chile Pasilla-Ancho pouches due to unlabeled peanut allergen.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jun 27, 2019.

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Compare the exact product and package details with the label you have.

ProductEl Guapo Pasilla-Ancho Chile Pods 2oz, 7.5oz, 11oz
Package size2oz
UPC044989010391, 044989211088, 044989211149

FDA code information

2oz: UPC# 044989010391; Best By Jun/20/20 7.5oz: UPC# 044989211088; Best By Jun/13/20; Best By Jun/14/20 11oz: UPC# 044989211149; Best By Jun/12/20

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Full FDA record and distribution details

Original product description

El Guapo Pasilla-Ancho Chile Pods 2oz, 7.5oz, 11oz

Extracted codes and context

TypeCode / valueContext
UPC0449890103912oz: UPC# 044989010391; Best By Jun/20/20 7.5oz: UPC# 044989211088; Best By Jun/13/20; Best By Jun/14/20 11oz: UPC# 044989211149; Best B
UPC0449892110882oz: UPC# 044989010391; Best By Jun/20/20 7.5oz: UPC# 044989211088; Best By Jun/13/20; Best By Jun/14/20 11oz: UPC# 044989211149; Best By Jun/12/20
UPC044989211149 7.5oz: UPC# 044989211088; Best By Jun/13/20; Best By Jun/14/20 11oz: UPC# 044989211149; Best By Jun/12/20

Original FDA recall reason

Mojave Foods Corporation (subsidiary of McCormick) is initiating a voluntary recall of El Guapo Chile Habanero and Chile Pasilla-Ancho pouches due to unlabeled peanut allergen.

Recall details

Recall number
F-1346-2019
Event ID
81938
FDA status
Terminated
Initiated
Jan 11, 2019
Reported
May 15, 2019
Classified
May 13, 2019
Terminated
Jun 27, 2019
Quantity
2 oz, 22,848 pouches ; 7.5oz, 13,896 pouches ; 11oz, 2,064 pouches
Location
Hunt Valley, MD, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Product distributed to the following states: AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN, IA, KS, KY, MI, MN, MO, MT, NE, NV, NM, NC, OH, OK, OR, TN, TX, UT, WI

FDA source record · F-1346-2019

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.