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Salmonella Test Prompts Asafoetida Powder Recall

By Denis Stearns on January 9, 2016

Pure-Asafoetida-PowderShakti Group USA LLC of New Brunswick, NJ is recalling 50 gm and 100 gm sizes of L.G Compounded Asafoetida Powder, both coded with Lot Number: 2323 because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

L.G COMPOUNDED ASAFOETIDA POWDER was distributed to OH, NJ, VA, NH, and PA through retail stores.

The product is packaged in a white screw cap plastic bottle with UPC 840222000149, Lot Number: 2323.

No illnesses have been reported to date.

The recall was as a result of a sampling conducted by the FDA, which revealed that the finished products contained the bacteria. Shakti Group has ceased the production and distribution of the product.

  • Posted in:
    Food, Drug & Agriculture, Personal Injury
  • Blog:
    Food Poison Journal
  • Organization:
    Marler Clark, Inc., PS
  • Article: View Original Source

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