CLASS II Food recall · Reported 22 Mar 2017 · FDA Enforcement Report

Choice Farms Pizza Style Portabella Mushrooms Individual recalled

Del Monte Fresh Produce N.A., Inc. HQ is recalling Choice Farms Pizza Style Portabella Mushrooms Individual, distributed in Kansas, Texas. The recall was initiated on 10 Feb 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSell by: 02/16/17
Quantity recalled124 trays

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-1605-2017
FDA event ID
76474
Recalling firm
Del Monte Fresh Produce N.A., Inc. HQ, Coral Gables, FL
Brand
Choice
Classification
Class II
Status
Terminated
Recall initiated
10 Feb 2017
FDA classified
14 Mar 2017
Reported
22 Mar 2017
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Listeria
Product category
Frozen Pizza

Timeline

10 Feb 2017Recall initiated by company
14 Mar 2017Classified by FDA+32 days
22 Mar 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

Possible contamination with 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

Choice Farms Pizza Style Portabella Mushrooms 8 oz. INDIVIDUAL SHRINK-WRAPPED TRAYS

Where it was distributed

Texas and Kansas

KansasTexas

Questions about this recall

Why was it recalled?

Possible contamination with Listeria monocytogenes.

Which lots are affected?

Sell by: 02/16/17

Where was it sold?

Texas and Kansas

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

2 other products · FDA event 76474

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