FDA recall record
Baidyanath brand Gaisantak Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P) Ltd. 1 Gupta Lane, Kolkata 700006
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of June 13, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Baidyanath brand Gaisantak 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.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Baidyanath brand Gaisantak Bati, Dietary Supplement, 80 Tablets -- Product of India --- Mfd in India - Shree Baidyanath Ayurved Bhawan (P) Ltd. 1 Gupta Lane, Kolkata 700006
Code information listed by FDA
Batch No. 1) GAI-09 & 2) 141, Expiry Date 1) 08/2018 & 2) 10/2017
Distribution and firm information
Recalling firm listed by FDA: Butala Emporium, Inc.
Firm location listed by FDA: Jackson Heights, NY, United States
Distribution reported by FDA: NY (via 3 retail stores) and directly to 26 individual consumers (CT, FL, HI, NJ, PA, OH, MA, District of Columbia, VT & PR)
Product quantity listed by FDA: 618 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.