FDA recall record

SHAKTI GROUP USA 1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT recall — FDA F-1121-2016

L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella.

Class Iclassification
F-1121-2016official record ID
Apr 27, 2016report date

Recall record at a glance

Official recordF-1121-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmSHAKTI GROUP USA LLC
Report dateApr 27, 2016
Recall initiation dateJan 7, 2016
Quantityapproximately 10000 bottles
LocationNew Brunswick, NJ, United States

Official product description

1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel Street, Mumbai - 400 003, (INDIA) MANUFACTURED AT: LALJEE GODHOO & CO. Plot No. 53/4, Road 7/15, M.I.D.C.,Andheri (E). Mumbai - 400 093. (INDIA) Lot No., Pkd & Best Before See Bottom LOT NO. 2323" 2) COMPOUNDED ASAFOETIDA POWDER L.G, NET WT. 100g (3.5OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel Street, Mumbai - 400 003, (INDIA) MANUFACTURED AT: LALJEE GODHOO & CO. Plot No. 53/4, Road 7/15, M.I.D.C., Andheri (E). Mumbai - 400 093. (INDIA) Lot No., Pkd & Best Before See Bottom LOT NO. 2323"

Why the product was recalled

L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella.

Distribution information

NH, NJ, PA, OH & VA

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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