Food Recall Check
Class I · High risk Terminated Initiated May 2, 2012 (14 years ago)

HEB Deli General Joes Chicken Entree recall

Recalled by He Butt Grocery Company · San Antonio, TX, United States

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

Why it was recalled

The product 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

HEB Deli General Joes Chicken Entree, UPC 0026966900000; HEB Deli HE Bowl General Joes Chicken, UPC 0026967400000; HEB Deli General Joe's Chicken Retail Pack, UPC 0026520900000; HEB Deli General Joes Chicken UPC 0026703700000

Quantity: unknown

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.

All product sold prior to 05/03/12.

Where it was sold

Texas

FDA's distribution note: TX

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
He Butt Grocery Company
Initiated by
Voluntary: Firm initiated
Recall initiated
May 2, 2012
In FDA report of
Feb 20, 2013
Terminated
Apr 10, 2013
FDA recall number
F-0992-2013 · event 61789
Official record
FDA enforcement report search

Also recalled with it (3 more products)

FDA files each product of one recall action separately; these share the same FDA event.