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
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
- Brand
- Marketside Grab
- 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 2017 | Recall initiated by company | |
| 4 Apr 2017 | Classified by FDA | +48 days |
| 12 Apr 2017 | Published 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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|---|---|---|---|---|---|
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