Kar's Sweet n' Salty Mix recall

Recalled by Kar Nut Products Company · Madison Heights, MI, United States

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

Why it was recalled

Possibility that the product may contain very small pieces of glass.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Kar's Sweet n' Salty Mix 3.5 oz. flexible film bags. 42 bags per case.

Quantity: 140,322 bags

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.

Product ID 8997 UPC: 077034089974 Best By dates: 08/25/15 thru 09/01/15 Lot #'s: WO0020171

Where it was sold

Alabama Arkansas Arizona California Colorado Connecticut Florida Georgia Iowa Illinois Indiana Kansas Kentucky Louisiana Maryland Maine Michigan Minnesota Missouri Mississippi North Carolina New Hampshire New Jersey Nevada New York Ohio Oklahoma Oregon Pennsylvania South Carolina Tennessee Texas Utah Virginia Washington Wisconsin

FDA's distribution note: US Only: AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MD, ME, MI, MN, MO, MS, NC, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI.

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: Kar Nut Products Company
Initiated by: Voluntary: Firm initiated
Recall initiated: Oct 19, 2015
In FDA report of: Nov 25, 2015
Terminated: Sep 27, 2016
FDA recall number: F-0154-2016 · event 72497
Official record: FDA enforcement report search

Also recalled with it (10 more products)

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

Class II · Moderate risk Terminated Foreign material Oct 19, 2015