Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 28, 2016 (10 years ago)

Joe Chips Retro Potato Chips Sour Cream & Toasted Onion Distributed by recall

Recalled by The Two Little Guys Company · Montclair, NJ, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Joe Chips Sour Cream & Toasted Onion Retro Potato Chips contains a seasoning with a milk powder ingredient that may be contaminated with Salmonella although firm testing has not revealed the presence of the bacteria.

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

Joe Chips Retro Potato Chips Sour Cream & Toasted Onion Distributed by: The Joe Tea Company, Upper Montclair, NJ 07043-0255 (973)744-7502 Net Wt. 2 OZ UPC 743234001725 Net Wt. 5 OZ UPC 743234001800

Quantity: 70,130 bags

Food: Milk & dairy Chips & snacks Onions

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.

expiration 2 oz size 27-MARCH-2017 THRU 09-JUL-2017 5 oz size 28-AUG-2017 THRU 19-NOV-2017

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
The Two Little Guys Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 28, 2016
In FDA report of
Feb 22, 2017
Terminated
Sep 28, 2017
FDA recall number
F-1480-2017 · event 76164
Official record
FDA enforcement report search

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