FDA Food recall F-1814-2017
Baidyanath brand Agnitundi Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P)…
- FDA Food
- Class I
- terminated
- Published 2017-04-05
On 2017-04-05 the FDA classified a Class I recall of Baidyanath brand Agnitundi Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P)… by Butala Emporium, citing the dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-1814-2017 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2015-08-27 |
| Published | 2017-04-05 |
| Last updated | 2026-09-13 11:49 UTC |
| Company | Butala Emporium |
| Distribution | CT, DC, FL, HI, MA, NJ, NY, OH, PA, PR, VT |
Product
Baidyanath brand Agnitundi Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P) Ltd. 1 Gupta Lane, Kolkata 700006
Reason
The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Identifiers
| code_info | Batch No. 018, Expiry Date 02/2016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:49 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1814-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.