All American Trading Of Houston, INC. Recall History
All American Trading Of Houston, INC. has had 1 FDA-tracked food recall since 2025. 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 2025
- Class I (Most Serious)
- 0
- Most Common Reason
- N/A
- Latest Recall
- Apr 4, 2025
- First Recorded Recall
- Apr 4, 2025
- States Affected
- MS, TX
- Currently Active
- 1
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every All American Trading Of Houston, 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 |
|---|---|---|---|
| Apr 4, 2025 | Texas Olive Co. Pepperoncini 16 oz glass jars | Class II | Active |
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, All American Trading Of Houston, INC. has 1 FDA food recall on record, including 0 Class I (dangerous) recalls. There is currently 1 active recall.
All American Trading Of Houston, INC. currently has 1 active recall. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.
All American Trading Of Houston, INC.'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.
All American Trading Of Houston, INC. recalls have affected MS, 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.
For readers using this page as a decision input, the related-entity pages elsewhere on the site provide the comparison set. The most useful comparison for this entity is typically a peer within U.S. consumer-product recalls with similar size, similar exposure, or similar geography — not the national-level summary alone.