Baidyanath brand Sarivadi Bati
Reason The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits .
Baidyanath brand Chitrakadi Bati recall
Recalled by Butala Emporium, Inc. · Jackson Heights, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.
What was recalled
Baidyanath brand Chitrakadi Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P) Ltd. 1 Gupta Lane, Kolkata 700006
Quantity: 169 bottles
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Batch No. 193, Expiry Date 02/2018
Where it was sold
Connecticut District of Columbia Florida Hawaii Massachusetts New Jersey New York Ohio Pennsylvania Puerto Rico Vermont
FDA's distribution note: NY (via 3 retail stores) and directly to 26 individual consumers (CT, FL, HI, NJ, PA, OH, MA, District of Columbia, VT & PR)
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Butala Emporium, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 27, 2015
- In FDA report of
- Apr 5, 2017
- Terminated
- Jun 13, 2018
- FDA recall number
- F-1818-2017 · event 72087
- Official record
- FDA enforcement report search
Also recalled with it (9 more products)
FDA files each product of one recall action separately; these share the same FDA event.
Baidyanath brand Rajahpravartini Bati
Reason The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits .
Baidyanath brand Saptamrit Lauh
Reason The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Baidyanath brand Shankh Bati
Reason The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Baidyanath brand Marichyadi Bati
Reason The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Baidyanath brand Agnitundi Bati
Reason The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Baidyanath brand Arogyavardhini Bati
Reason The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Baidyanath brand Brahmi Bati
Reason The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.
Baidyanath brand Gaisantak Bati
Reason The dietary supplements were found to contain lead, mercury and/or arsenic at levels exceeding permissible limits.