Radhuni Curry Powder recall
Recalled by New Hoque & Sons, Inc. · Maspeth, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Curry powder is contaminated with Salmonella spp. detected by FDA sampling.
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
"Radhuni Curry Powder, 400 grams (14.11 oz.)***Ingredients: Coriander, Tumeric, Chili, Bitsalt, Aniseed, Sodium Chloride, Garlic, Cumin, Bay leaf, Ginger, Cinnamon, Clove, Cardamon***Product of Bangladesh***Imported by New Hoque & Sons Inc., NY USA***"
Quantity: 33 cases
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.
Batch #: 20010245 UPC code: 8941100510735 Manufacturing Date (MFG): 02 January 2020 Best Before (BB)/Expiration (EXP) Date: 02 January 2022
Where it was sold
New York
FDA's distribution note: Product imported from Bangladesh and distributed in NY state.
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
- New Hoque & Sons, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 14, 2020
- In FDA report of
- Jul 1, 2020
- Terminated
- Mar 30, 2021
- FDA recall number
- F-0999-2020 · event 85710
- Official record
- FDA enforcement report search