Butala Emporium, INC. Recall History
Butala Emporium, INC. has had 2 FDA-tracked food recalls since 2015, including 2 Class I recalls (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
- 2
- Years in FDA Data
- Since 2015
- Class I (Most Serious)
- 2
- Most Common Reason
- N/A
- Latest Recall
- Aug 27, 2015
- First Recorded Recall
- Aug 27, 2015
- States Affected
- 11 states (nationwide)
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (2 Records)
Every Butala Emporium, 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 |
|---|---|---|---|
| Aug 27, 2015 | Baidyanath brand Saptamrit Lauh, Dietary Supplement, 80 ... | Class I | Terminated |
| Aug 27, 2015 | Baidyanath brand Marichyadi Bati, Dietary Supplement, 80 ... | 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, Butala Emporium, INC. has 2 FDA food recalls on record, including 2 Class I (dangerous) recalls. There are no active recalls at this time.
Butala Emporium, INC. has no active recalls at this time. However, the brand has 2 historical recalls. Always check this page for the latest recall status.
Butala Emporium, INC.'s 2 recalls break down by severity: 2 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.
Butala Emporium, INC. recalls have affected 11 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).
this entity is one of the data points covered by this site’s U.S. FDA food, drug, and device recalls dataset. The detail above comes directly from the FDA openFDA enforcement-report API; the context that follows situates the headline numbers against the broader distribution across U.S. consumer-product recalls.
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.
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.