Heinens Organic Nut Mix recall

Recalled by Ohio Hickory Harvest Brand Products Inc. · Akron, OH, United States

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

Why it was recalled

The firm received positive test results for Listeria monocytogenes in a product that was housed in the same storage bin.

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

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

Heinens Organic Nut Mix Net Wt. 9 oz (255g) Distributed By Heinens, Warrensville Hts., OH 44128 UPC 0-36232-01871-1

Quantity: 40 Cases with 6 tubs per case

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.

Lot # 031919

Where it was sold

Alabama Arkansas Arizona California Colorado Connecticut Florida Georgia Iowa Illinois Indiana Kansas Kentucky Louisiana Maryland Michigan Missouri North Carolina North Dakota Nebraska Nevada New York Ohio Oklahoma Oregon Pennsylvania South Carolina Tennessee Texas Utah Virginia Washington Wyoming

FDA's distribution note: Product was only distributed in the following states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MD, MI, MO, NC, ND, NE, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA and WY.

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: Ohio Hickory Harvest Brand Products Inc.
Initiated by: Voluntary: Firm initiated
Recall initiated: Apr 10, 2018
In FDA report of: Jun 6, 2018
Terminated: Jul 16, 2018
FDA recall number: F-1496-2018 · event 79714
Official record: FDA enforcement report search