McCormick & Company - Corporate Headquarters Recall History
McCormick & Company - Corporate Headquarters has had 1 FDA-tracked food recall since 2016. The full list below — sourced from the FDA openFDA enforcement database — shows dates, products, reasons, and classifications for every recall on record.
Key Facts
- Total Recalls
- 1
- Years in FDA Data
- Since 2016
- Class I (Most Serious)
- 0
- Most Common Reason
- N/A
- Latest Recall
- Aug 12, 2016
- First Recorded Recall
- Aug 12, 2016
- States Affected
- 23 states (nationwide)
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every McCormick & Company - Corporate Headquarters recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.
| Date | Product | Class | Status |
|---|---|---|---|
| Aug 12, 2016 | ZATARAINS WHITE CHEDDAR CHIPOTLE PASTA DINNER 6 OZ PACKAGE | Class II | Terminated |
Recall data sourced from the FDA's recalls and safety alerts database. Class I recalls indicate a reasonable probability of serious adverse health consequences. Always check the USDA FSIS recall list for meat and poultry products.
Frequently Asked Questions
Yes, McCormick & Company - Corporate Headquarters has 1 FDA food recall on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.
McCormick & Company - Corporate Headquarters has no active recalls at this time. However, the brand has 1 historical recall. Always check this page for the latest recall status.
McCormick & Company - Corporate Headquarters's 1 recall break down by severity: 0 Class I (may cause serious health issues), 1 Class II (may cause temporary health problems), and 0 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
McCormick & Company - Corporate Headquarters recalls have affected 23 states (nationwide distribution). Check individual recall entries for specific distribution details.
Related
Recall data is sourced from the FDA openFDA enforcement database. Classifications reflect FDA severity ratings: Class I (dangerous), Class II (may cause temporary health problems), Class III (unlikely harmful).
The this entity record above pulls directly from the FDA openFDA enforcement-report API. What follows is the per-entity context — how this entity sits in the broader U.S. FDA food, drug, and device recalls distribution and which underlying factors drive the headline numbers.
The methodology behind every numeric value on this page is publicly documented on the the FDA openFDA enforcement-report API portal and described in detail on this site’s methodology page. Refresh cadence varies by underlying series; the page surfaces the as-of date for each number so readers can trace any figure back to the source release.
Practical use of this page is in combination with the comparison and ranking pages elsewhere on the site, which surface the same data for this entity’s peers within U.S. consumer-product recalls. A single-entity reading without peer context can be misleading when an entity is an outlier on one axis but typical on another.