CLASS II Food recall · Reported 1 Feb 2017 · FDA Enforcement Report

Everroast Chicken Caesar Wrap recalled by Harris Teeter

Harris Teeter is recalling Everroast Chicken Caesar Wrap, distributed in 8 states. The recall was initiated on 6 Jan 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll code dates

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-1367-2017
FDA event ID: 76188
Recalling firm: Harris Teeter, Matthews, NC
Brand: Everroast
Classification: Class II
Status: Terminated
Recall initiated: 6 Jan 2017
FDA classified: 26 Jan 2017
Reported: 1 Feb 2017
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Undeclared Allergens
Product category: Ready Meals

Timeline

6 Jan 2017	Recall initiated by company
26 Jan 2017	Classified by FDA	+20 days
1 Feb 2017	Published in enforcement report	+6 days

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

Reason for recall

Undeclared allergen (fish)

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

Everroast Chicken Caesar Wrap, UPC: 72036-95828, in clear flexible plastic.

Where it was distributed

DC, DE, FL, GA, MD, NC, SC, VA.

District of Columbia Delaware Florida Georgia Maryland North Carolina South Carolina Virginia

Stores named: Kroger

Questions about this recall

Why was it recalled?

Undeclared allergen (fish)

Which lots are affected?

All code dates

Where was it sold?

DC, DE, FL, GA, MD, NC, SC, 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.

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