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SHAKTI GROUP USA LLC recall - 1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.),…
FDA (enforcement) · April 27, 2016 · Class I
- SHAKTI GROUP USA LLC recalled 1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.), MANUFACTURED BY: LALJEE… - an FDA enforcement event posted , classified Class I, covering 1 product entry.
- FDA-stated reason: L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella.
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class I
- Status
- Terminated
- Recalling firm
- SHAKTI GROUP USA LLC
- Source ID
- 73020
FDA Enforcement Report search →
How this recall compares
- Shakti Group Usa Llc has 2 recall events in the FDA (2012+) and USDA-FSIS (2014+) records tracked here; by posting date this is the 2nd. The one before it: SHAKTI GROUP USA LLC recall - Cumin Ground Product of India 50 lbs C/7784 ().
- It is one of 11 Salmonella recall events FDA and USDA-FSIS posted in April 2016 (all Salmonella recalls).
Product entries (1)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| F-1121-2016 | 1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.), MANUFACTURED BY: LALJEE GODHOO & CO. 213, Samuel Street, Mumbai - 400 003, (INDIA) MANUFACTURED… | Lot 2323 | NH, NJ, PA, OH & VA |
FDA enforcement entries have no per-recall public URL - verify via the FDA Enforcement Report search using the firm name or a recall number above.
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