Food Recall Check
Class I · High risk Terminated Initiated Oct 23, 2018 (8 years ago)

Inshell R/S 21/25 US- Select Pistachios recall

Recalled by Sam Dry Fruits and Enterprises Inc. · Modesto, CA, United States

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

Why it was recalled

Positive result for Salmonella received while investigating to determine supplier of direct customer's positive findings also for 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

Inshell R/S 21/25 US- Select Pistachios; NET WT. 25 lb. (11.34kg) Product of the USA Production Date: 8/2018 ARO Pistachios Inc. 19750 Avenue 88, Terra Bella, CA 93270

Quantity: 18, 225 lbs.

Food: Nuts & seeds

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 number: RS100119. Best By 2/2020

Where it was sold

Maryland New Jersey New York Pennsylvania

FDA's distribution note: NJ, MD, NY, PA, NJ

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
Sam Dry Fruits and Enterprises Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 23, 2018
In FDA report of
Nov 14, 2018
Terminated
May 7, 2019
FDA recall number
F-0617-2019 · event 81406
Official record
FDA enforcement report search

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