Food Recall Check
Class I · High risk Terminated Initiated Jul 22, 2016 (10 years ago)

Primo Fresh Serrano Peppers Distributed by Warren Produce recall

Recalled by Warren Produce Co., LLC · Edinburg, TX, United States

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

Why it was recalled

Product tested positive 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

Primo Fresh Serrano Peppers Distributed by Warren Produce, 824 W. Monte Cristo Rd, Edinburg, TX packaged in 1/4 bushel waxed cardboard boxes, 1 1/9 bushel waxed cardboard boxes, 10 lb waxed cardboard boxes, 5 lb waxed cardboard boxes and 35 lb RPC crates.

Quantity: 14,000 pounds

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.

115158, 115181, 115186

Where it was sold

California Colorado Georgia Indiana Kansas Louisiana Missouri New York Oklahoma Texas

FDA's distribution note: TX, OK, KS, GA, CA, LA, IN, CO, MO, NY

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
Warren Produce Co., LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 22, 2016
In FDA report of
Sep 7, 2016
Terminated
Dec 28, 2016
FDA recall number
F-2036-2016 · event 74789
Official record
FDA enforcement report search