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

Lot, batch or date codesBatch No. 018, Expiry Date 02/2016
Quantity recalled173 bottles

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
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 2015Recall initiated by company
30 Mar 2017Classified by FDA+581 days
5 Apr 2017Published 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 72087

This product is part of a recall event; the main page for the event is Baidyanath Saptamrit Lauh, Dietary Supplement recalled.

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