Cumin Ground Product of India
Reason Cumin contains 8.0 ppm peanut allergen.
1) Compounded Asafoetida Powder L.G.¿ recall
Recalled by Shakti Group USA LLC · New Brunswick, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
L.G. compounded Asafoetida powder has the potential to be contaminated with Salmonella.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
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"
Quantity: approximately 10000 bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot 2323
Where it was sold
New Hampshire New Jersey Ohio Pennsylvania Virginia
FDA's distribution note: NH, NJ, PA, OH & VA
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Shakti Group USA LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 7, 2016
- In FDA report of
- Apr 27, 2016
- Terminated
- Oct 23, 2017
- FDA recall number
- F-1121-2016 · event 73020
- Official record
- FDA enforcement report search