Baidyanath brand Brahmi Bati — Class I food recall F-1816-2017
Terminated recall by Butala Emporium, Inc., reported 2017-04-05, distributed in CT, DC, FL, HI, MA, NJ, NY, OH…. The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible lim
| Recall number | F-1816-2017 |
|---|---|
| Product type | Food |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Butala Emporium, Inc., Jackson Heights, NY, United States |
| Recall initiated | 2015-08-27 |
| Classified | 2017-03-30 |
| Reported by FDA | 2017-04-05 |
| Terminated | 2018-06-13 |
| Distributed | CT, DC, FL, HI, MA, NJ, NY, OH, PA, PR, VT |
| Quantity | 466 bottles |
| Reason classes | chemical contamination |
| Expiration dates | 2019-03 |
Product
Baidyanath brand Brahmi Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P) Ltd. 1 Gupta Lane, Kolkata 700006
Reason for recall
The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1816-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.