Reo Spice & Seasoning, INC Recall History
Reo Spice & Seasoning, INC has had 1 FDA-tracked food recall since 2014, including 1 Class I recall (most serious). 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 2014
- Class I (Most Serious)
- 1
- Most Common Reason
- Undeclared allergens (1)
- Latest Recall
- Dec 31, 2014
- First Recorded Recall
- Dec 31, 2014
- States Affected
- TX
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every Reo Spice & Seasoning, INC 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 |
|---|---|---|---|
| Dec 31, 2014 | Reo Ranch House Sizzling Steak Beef Jerky Seasoning Total... | Class I | 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, Reo Spice & Seasoning, INC has 1 FDA food recall on record, including 1 Class I (dangerous) recall. There are no active recalls at this time.
Reo Spice & Seasoning, INC has no active recalls at this time. However, the brand has 1 historical recall. Always check this page for the latest recall status.
Reo Spice & Seasoning, INC's 1 recall break down by severity: 1 Class I (may cause serious health issues), 0 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.
Reo Spice & Seasoning, INC recalls have affected TX. 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.
Every number on this page links back to the FDA openFDA enforcement-report API; the methodology page describes the inputs, refresh cadence, and known limitations of the underlying data product.
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.