Baidyanath Agnitundi Bati dietary supplements from India contain unsafe levels of lead, mercury, and arsenic. Consumers should stop using these products immediately due to potential health risks.
The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Baidyanath brand Agnitundi Bati dietary supplements were recalled because they contain unsafe levels of lead, mercury, and arsenic. These contaminants exceed permitted limits and could pose health risks to consumers.
The dietary supplements contain lead, mercury, and/or arsenic at levels exceeding permissible limits. These heavy metals can cause serious health issues, including neurological damage and organ failure, when consumed over time.
Anyone who owns or uses the Baidyanath Agnitundi Bati dietary supplements. People with pre-existing health conditions may be at higher risk due to the contaminants.
Look for the Baidyanath brand Agnitundi Bati dietary supplement with 80 tablets. The product was manufactured in India by Shree Baidyanath Ayurved Bhawan (P) Ltd. in Kolkata, with batch number 018 and an expiry date of February 2016.
Immediately stop using the Baidyanath Agnitundi Bati dietary supplements as they contain unsafe levels of lead, mercury, and arsenic.
The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Look for the Baidyanath brand Agnitundi Bati dietary supplement with 80 tablets. The product was manufactured in India by Shree Baidyanath Ayurved Bhawan (P) Ltd. in Kolkata, with batch number 018 and an expiry date of February 2016.
Immediately stop using the product and contact the manufacturer for further instructions.
We’ve drafted a message you can send Baidyanath to request your refund or repair — edit it as you like.
Subject: Recall F-1814-2017 — Baidyanath Baidyanath Hello, I own a Baidyanath that is covered by recall F-1814-2017 from Baidyanath. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
