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RECALLING FIRM / COMPANY

SHAKTI GROUP USA LLC Recalls

Are there any recent FDA recalls involving SHAKTI GROUP USA LLC?

0 recall records initiated in the snapshot’s last 365 days. 0 are FDA-listed ongoing with no termination date.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026

The FDA identifies this company as the recalling firm; this does not establish that it is the manufacturer, retailer or brand owner. “Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today.

2 FDA product recordsLatest initiation: Jan 7, 2016

Same product name.
Different batch.
Check the label.

Latest recalls involving SHAKTI GROUP USA LLC

Most recently initiated in the available FDA data; these are not necessarily active recalls.

Jan 7, 2016 · FDA status: Terminated1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.)L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella.View recall details →Aug 25, 2015 · FDA status: TerminatedCumin Ground Product of India 50 lbs C/7784Cumin contains 8.0 ppm peanut allergen.View recall details →

Earlier recall history

2 records initiated before 2026. Browse the history below or choose a year.

2016 (1)2015 (1)

All FDA recall records involving SHAKTI GROUP USA LLC

Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

2 recall recordsPage 1 of 1
Class I
FDA status: Terminated

1) COMPOUNDED ASAFOETIDA POWDER L.G.¿, NET WT. 50g (1.75OZ.)

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

SalmonellaView details →
Class II
FDA status: Terminated

Cumin Ground Product of India 50 lbs C/7784

Cumin contains 8.0 ppm peanut allergen.

Undeclared allergenView details →

Found your product? Now check the codes.

Same product name. Different batch. Details matter.

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