1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.)
Recalling firm: SHAKTI GROUP USA LLC
L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 23, 2017.
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FDA code information
Lot 2323
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Full FDA record and distribution details
Original 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"
Original FDA recall reason
L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella.
Recall details
- Recall number
- F-1121-2016
- Event ID
- 73020
- FDA status
- Terminated
- Initiated
- Jan 7, 2016
- Reported
- Apr 27, 2016
- Classified
- Apr 20, 2016
- Terminated
- Oct 23, 2017
- Quantity
- approximately 10000 bottles
- Location
- New Brunswick, NJ, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
NH, NJ, PA, OH & VA
Data updated September 16, 2026. View official FDA data ↗
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