CLASS II Food recall · Reported 7 Mar 2018 · FDA Enforcement Report

Vareniki Cabbage recalled by M & P Food Productions

M & P Food Productions is recalling Vareniki Cabbage, distributed in 10 states. The recall was initiated on 16 Feb 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUse By Dates: 02/16/2018 - 08/15/2018
Quantity recalledUnknown

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-0836-2018
FDA event ID
79258
Recalling firm
M & P Food Productions, Brooklyn, NY
Classification
Class II
Status
Terminated
Recall initiated
16 Feb 2018
FDA classified
26 Feb 2018
Reported
7 Mar 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Product category
Other

Timeline

16 Feb 2018Recall initiated by company
26 Feb 2018Classified by FDA+10 days
7 Mar 2018Published in enforcement report+9 days

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

Reason for recall

Product contains undeclared wheat.

Product as listed by the FDA

M&P Food Productions brand Vareniki Cabbage, Net WT 14 oz. (396g), Keep Frozen, UPC: 7 07163 02619 8

Where it was distributed

NY, CT, KS, FL, SC, MA, NJ, PA, OK, VA

ConnecticutFloridaKansasMassachusettsNew JerseyNew YorkOklahomaPennsylvaniaSouth CarolinaVirginia

Questions about this recall

Why was it recalled?

Product contains undeclared wheat.

Which lots are affected?

Use By Dates: 02/16/2018 - 08/15/2018

Where was it sold?

NY, CT, KS, FL, SC, MA, NJ, PA, OK, VA

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

6 other products · FDA event 79258

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