CLASS I Food recall · Reported 12 Apr 2017 · FDA Enforcement Report

Marketside Grab and Go No Smoke Provolone Set Ups recalled

Biery Cheese is recalling Marketside Grab and Go No Smoke Provolone Set Ups, distributed in 11 states. The recall was initiated on 15 Feb 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesItem 12901 Best By: 04/01/17, 04/02/17, 04/25/17 & 04/26/17.
Quantity recalled3914 cases of 11 / 10.8 oz packages

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1847-2017
FDA event ID
76493
Recalling firm
Biery Cheese, Louisville, OH
Classification
Class I
Status
Terminated
Recall initiated
15 Feb 2017
FDA classified
4 Apr 2017
Reported
12 Apr 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Listeria
Product category
Ready Meals

Timeline

15 Feb 2017Recall initiated by company
4 Apr 2017Classified by FDA+48 days
12 Apr 2017Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The firm was notified by their supplier that various cheese products test positive for Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Marketside Grab and Go No Smoke Provolone 10.8 oz Set Ups

Where it was distributed

Product was shipped to the following states: FL, GA, IL, IN, KY, MA, MI, NJ, OH, PA & WI.

FloridaGeorgiaIllinoisIndianaKentuckyMassachusettsMichiganNew JerseyOhioPennsylvaniaWisconsin

Stores named: Walmart

Questions about this recall

Is Marketside Grab and Go No Smoke Provolone Set Ups recalled?

Yes. Biery Cheese recalled Marketside Grab and Go No Smoke Provolone Set Ups on 15 Feb 2017. The recall is Class I and its status is Terminated. Recall number F-1847-2017.

Why was it recalled?

The firm was notified by their supplier that various cheese products test positive for Listeria monocytogenes.

Which lots are affected?

Item 12901 Best By: 04/01/17, 04/02/17, 04/25/17 & 04/26/17.

Where was it sold?

Product was shipped to the following states: FL, GA, IL, IN, KY, MA, MI, NJ, OH, PA & WI.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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