# FDA recall F-1121-2016

> **SHAKTI GROUP USA LLC** · Class I · food recall initiated 2016-01-07.

## Product

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"

## Reason for recall

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

## Distribution

NH, NJ, PA, OH & VA

## Key facts

- **Recall number:** F-1121-2016
- **Recalling firm:** SHAKTI GROUP USA LLC
- **Classification:** Class I
- **Product type:** food
- **Status:** Terminated
- **Initiation date:** 2016-01-07
- **Report date:** 2016-04-27
- **Termination date:** 2017-10-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New Brunswick, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=F-1121-2016

## Citation

> AI Analytics. FDA recall F-1121-2016. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/F-1121-2016. Source: US FDA. Licensed CC0.

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