Food Recall Check
Class I · High risk Terminated Initiated Dec 19, 2017 (9 years ago)

Haldiram's Fresh Paneer Traditional Indian Soft Cottage Cheese recall

Recalled by Kotecha Brothers, LLC. · Miami, FL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Florida Department of Agriculture and Consumer Services (FDACS) collected a sample of Fresh Paneer Traditional Indian Soft Cottage Cheese 100% Vegetarian from a local grocery store that tested positive for Listeria monocytogenes. The sample was imported by Kotecha Brothers LLC.

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

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

Haldiram's Fresh Paneer Traditional Indian Soft Cottage Cheese, Net Weight 800g (28.2 oz)

Quantity: 45 cases

Food: Cheese

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 No. 26 GQ (KB) Best Before 07/28/2018

Where it was sold

Florida

FDA's distribution note: Florida consignees only.

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
Kotecha Brothers, LLC.
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 19, 2017
In FDA report of
Jan 17, 2018
Terminated
Aug 27, 2019
FDA recall number
F-0564-2018 · event 78814
Official record
FDA enforcement report search

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