FDA Recall United States Terminated Historical recordClass II
McCormick & Company - Corporate Headquarters
- Product
- ZATARAINS GUMBO PASTA DINNER 5.7 OZ PACKAGE
- Published
- September 28, 2016
- Distribution
- Product shipped to the following states:…
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.
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.
- - Recall initiated
- - Reported by source
- - Recall terminated
| 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
Other recalls from McCormick & Company - Corporate Headquarters
FDA Recall United States Terminated Historical recordClass II
McCormick & Company - Corporate Headquarters
- Product
- ZATARAINS SCAMPI PASTA DINNER 5.2 OZ PACKAGE
- Published
- September 28, 2016
- Distribution
- Product shipped to the following states:…
FDA Recall United States Terminated Historical 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:…
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.
| 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.
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?
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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.
