CLASS I Food recall · Reported 5 Apr 2017 · FDA Enforcement Report
Baidyanath Agnitundi Bati, Dietary Supplement recalled
Butala Emporium is recalling Baidyanath Agnitundi Bati, Dietary Supplement, distributed in 11 states. The recall was initiated on 27 Aug 2015 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1814-2017
- FDA event ID
- 72087
- Recalling firm
- Butala Emporium, Jackson Heights, NY
- Brand
- Baidyanath Agnitundi
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 27 Aug 2015
- FDA classified
- 30 Mar 2017
- Reported
- 5 Apr 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Lead & Heavy Metals
- Product category
- Dietary Supplements
Timeline
| 27 Aug 2015 | Recall initiated by company | |
| 30 Mar 2017 | Classified by FDA | +581 days |
| 5 Apr 2017 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Lead and other heavy metals accumulate in the body. Children are most at risk; even low levels can affect development.
Product as listed by the FDA
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
Where it was distributed
NY (via 3 retail stores) and directly to 26 individual consumers (CT, FL, HI, NJ, PA, OH, MA, District of Columbia, VT & PR)
ConnecticutDistrict of ColumbiaFloridaHawaiiMassachusettsNew JerseyNew YorkOhioPennsylvaniaPuerto RicoVermont
Questions about this recall
Why was it recalled?
The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Which lots are affected?
Batch No. 018, Expiry Date 02/2016
Where was it sold?
NY (via 3 retail stores) and directly to 26 individual consumers (CT, FL, HI, NJ, PA, OH, MA, District of Columbia, VT & PR)
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
9 other products · FDA event 72087This product is part of a recall event; the main page for the event is Baidyanath Saptamrit Lauh, Dietary Supplement recalled.
More recalls from Butala Emporium
All 10| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | Baidyanath Brahmi Bati, Dietary Supplement recalled by Butala EmporiumBaidyanath Brahmi | Butala Emporium | Lead & Heavy Metals | 11 states |
| Food | CLASS I | Baidyanath Shankh Bati, Dietary Supplement recalled by Butala EmporiumBaidyanath Shankh | Butala Emporium | Lead & Heavy Metals | 11 states |
| Food | CLASS I | Baidyanath Gaisantak Bati, Dietary Supplement recalledBaidyanath Gaisantak | Butala Emporium | Lead & Heavy Metals | 11 states |
| Food | CLASS I | Baidyanath Rajahpravartini Bati, Dietary Supplement recalledBaidyanath Rajahpravartini | Butala Emporium | Lead & Heavy Metals | 11 states |
| Food | CLASS I | Baidyanath Arogyavardhini Bati, Dietary Supplement recalledBaidyanath Arogyavardhini | Butala Emporium | Lead & Heavy Metals | 11 states |
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