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McCormick & Company - Corporate Headquarters Recall: The Zatarains plant in Gretna, LA was contacted by General Mills to inform the plant that they were impacted by General Mills flour recall. Fifty (50) bags of WONDRA ENR 50 UNMALTED were shipped to Gretna in March 2016. This material has been used in the production of four different Zatarains brand pasta dinner mixes over several processing dates. - F-2326-2016

United States

TerminatedClass II

Company
McCormick & Company - Corporate Headquarters
Product
ZATARAINS SOUTHERN STROGANOFF PASTA DINNER 6.5 OZ. PACKAGE
Recall date
August 12, 2016
Terminated
January 26, 2017
Source
FDA

Reason for recall

The Zatarains plant in Gretna, LA was contacted by General Mills to inform the plant that they were impacted by General Mills flour recall. Fifty (50) bags of WONDRA ENR 50 UNMALTED were shipped to Gretna in March 2016. This material has been used in the production of four different Zatarains brand pasta dinner mixes over several processing dates.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
ZATARAINS SOUTHERN STROGANOFF PASTA DINNER 6.5 OZ. PACKAGE Not published in this source record Not published in this source record Not published in this source record

Distribution

  • Product shipped to the following states: AL
  • AR
  • AZ
  • CA
  • DE
  • FL
  • GA
  • IA
  • IL
  • IN
  • KY
  • LA
  • MD
  • MS
  • NC
  • OR
  • PA
  • SC
  • TN
  • TX
  • VA
  • WA
  • and WI . Other Countries: Curacao

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2326-2016
Status
Terminated
Classification
Class II
Company
McCormick & Company - Corporate Headquarters
Product description
ZATARAINS SOUTHERN STROGANOFF PASTA DINNER 6.5 OZ. PACKAGE
Quantity
Not published in this source record
Reason
The Zatarains plant in Gretna, LA was contacted by General Mills to inform the plant that they were impacted by General Mills flour recall. Fifty (50) bags of WONDRA ENR 50 UNMALTED were shipped to Gretna in March 2016. This material has been used in the production of four different Zatarains brand pasta dinner mixes over several processing dates.
Recall initiation date
August 12, 2016
Report date
September 28, 2016
Classification date
Not published in this source record
Termination date
January 26, 2017
Distribution pattern
Product shipped to the following states: AL, AR, AZ, CA, DE, FL, GA, IA, IL, IN, KY, LA, MD, MS, NC, OR, PA, SC, TN, TX, VA, WA, and WI . Other Countries: Curacao
UPC, lot, and code information
Not published in this source record
Voluntary or mandated
Not published in this source record
Initial notification method
Not published in this source record
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: McCormick & Company - Corporate Headquarters

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Product
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Published
September 28, 2016
Distribution
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Product
ZATARAINS SCAMPI PASTA DINNER 5.2 OZ PACKAGE
Published
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Distribution
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FDA Recall United States TerminatedTerminated: January 26, 2017Historical recordClass II

McCormick & Company - Corporate Headquarters

Product
ZATARAINS WHITE CHEDDAR CHIPOTLE PASTA DINNER 6 OZ PACKAGE
Published
September 28, 2016
Distribution
Product shipped to the following states:…

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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
Alabama 1
Arkansas 1
Arizona 1
California 1
Delaware 1
Florida 1
Georgia 1
Iowa 1
Illinois 1
Indiana 1
Kentucky 1
Louisiana 1
Maryland 1
Mississippi 1
North Carolina 1
Oregon 1
Pennsylvania 1
South Carolina 1
Tennessee 1
Texas 1
Virginia 1
Washington 1
Wisconsin 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.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

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?

FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of January 26, 2017.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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.

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