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Data / Product recalls / Shakti Group USA LLC

Shakti Group USA LLC: 2 recalls from 2015 to 2016 (FDA)

Shakti Group USA LLC, New Brunswick, NJ, is named in 2 recalls from 2015 to 2016: all from the FDA. The latest, on April 27, 2016, covers 1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel Street.... Hazard: L.G. Source: FDA F-1121-2016.

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Country
United States
Location
New Brunswick, NJ
Agencies
U.S. Food and Drug Administration
First recall
December 9, 2015
Latest recall
April 27, 2016

Recalls

Each recall is listed once, with the role this firm has in it. Roles: recalling firm (2).

DateAgencyProductHazardUnitsRemedySold atRoleSource
April 27, 2016FDA1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel Street, Mumbai - 400 003, (INDIA)...L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella.approximately 10000 bottlesVoluntary recall, Class I, terminatedRecalling firmaccessdata.fda.gov
December 9, 2015FDACumin Ground Product of India 50 lbs C/7784Cumin contains 8.0 ppm peanut allergen.39,450 lbsVoluntary recall, Class II, terminatedRecalling firmaccessdata.fda.gov

By agency

AgencyRecallsLatest
U.S. Food and Drug Administration2April 27, 2016

Where each agency publishes its recalls

Updated April 27, 2016. Read from U.S. Food and Drug Administration recall data. CC0 1.0 (openFDA). Recalls are as the agencies published them: the CPSC, FDA (food enforcement reports) and NHTSA. A firm is one firm only when its exact name and country match; the CPSC and FDA print no firm ID. Stores are listed only when the agency's sold-at text names them, and an agency often adds that more stores sold the product. Categories are grouped by SpecStream from the words in the agency's title and product text. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.