Drug recall
1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel…
FDA recall event 73020 · Class I · SHAKTI GROUP USA LLC
Key facts
| Event ID | 73020 |
|---|---|
| Recall numbers | F-1121-2016 |
| Recalling firm | SHAKTI GROUP USA LLC |
| Product type | Food |
| Products | 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… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella. |
| Initiation date | Jan 7, 2016 |
| Report date | Apr 27, 2016 |
| Termination date | Oct 23, 2017 |
| City | New Brunswick |
| State | NJ |
| Country | United States |
| FEI number | 3011169006 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: