Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 19, 2016 (10 years ago)

Buffalo Blue Kettle Cooked Potato Chips recall

Recalled by Pinnacle Foods · Berlin, PA, United States

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

Why it was recalled

Snyder of Berlin is recalling their Buffalo Blue Kettle Cooked Potato Chips after being informed that a milk powder used within a spice blend ingredient may contain 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

Buffalo Blue Kettle Cooked Potato Chips 8 oz (227g)

Quantity: 17, 085 units.

Food: Chips & snacks

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.

UPC 023000439229 Product Codes: FEB2117M77A, FEB2117H44A, FEB2117H44B, FEB2817H77A, MAR0717H77A, MAR2117M77A

Where it was sold

Indiana Kentucky Maryland New York Ohio Pennsylvania Tennessee Virginia West Virginia

FDA's distribution note: IN, KY, MD, NY, OH, PA, TN, VA, WV

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. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. 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
Pinnacle Foods
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 19, 2016
In FDA report of
Apr 5, 2017
Terminated
Jul 14, 2017
FDA recall number
F-1726-2017 · event 76019
Official record
FDA enforcement report search

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