CLASS I Food recall · Reported 24 Jul 2013 · FDA Enforcement Report

QFC Chicken Pesto Panini wrapped in polywrap packaging recalled

Kroger is recalling QFC Chicken Pesto Panini wrapped in polywrap packaging in size, included with five other, distributed in Oregon, Washington. The recall was initiated on 22 Jun 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesThe affected product has a sell by date of 06/22/13 and a UPC code of 1111039114.

Quantity recalled235 sandwiches

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-1718-2013
FDA event ID: 65566
Recalling firm: Kroger, Cincinnati, OH
Classification: Class I
Status: Terminated
Recall initiated: 22 Jun 2013
FDA classified: 17 Jul 2013
Reported: 24 Jul 2013
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Undeclared Allergens
Product category: Ready Meals

Timeline

22 Jun 2013	Recall initiated by company
17 Jul 2013	Classified by FDA	+25 days
24 Jul 2013	Published in enforcement report	+7 days

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

Reason for recall

The paninis may contain soy and egg, which are allergens.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

QFC Chicken Pesto Panini wrapped in polywrap packaging, 10.32 oz. in size, included with five (5) other types of sandwiches in a 6-count "variety pack" case.

Where it was distributed

The affected product was only distributed in the states of WA and OR.

Oregon Washington

Stores named: Kroger

Questions about this recall

Why was it recalled?

The paninis may contain soy and egg, which are allergens.

Which lots are affected?

The affected product has a sell by date of 06/22/13 and a UPC code of 1111039114.

Where was it sold?

The affected product was only distributed in the states of WA and OR.

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 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.

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