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Lower risk Food recall · FDA · Published January 6, 2017

Harris Teeter Everroast Chicken Caesar Wrap Recall: Undeclared Fish Allergen

Harris Teeter recalls Everroast Chicken Caesar Wrap (UPC 72036-95828) due to undeclared fish allergen. Consumers should avoid this product to prevent allergic reactions.

🇺🇸 FDA recall #F-1367-2017FoodHarris Teeter ›
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Recalling firmHarris Teeter701 Crestdale Rd · Matthews, NC 28105-1700
✎ GovInfoNow plain-language explainer

What happened, in plain English

Harris Teeter is recalling Everroast Chicken Caesar Wraps with UPC 72036-95828 because they contain fish, an allergen that wasn't declared on the label. This poses a risk for people with fish allergies who might consume the product without knowing. Read more at govinfonow.com/recall/22460-harris-teeter-everroast-chicken-caesar-wrap-recall-undeclared-fish-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/22460-harris-teeter-everroast-chicken-caesar-wrap-recall-undeclared-fish-allergen · Updated October 8, 2026 · FDA enforcement record: FDA #F-1367-2017

Cite this page

“Harris Teeter Everroast Chicken Caesar Wrap Recall: Undeclared Fish Allergen.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22460-harris-teeter-everroast-chicken-caesar-wrap-recall-undeclared-fish-allergen. Based on FDA recall #F-1367-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1367-2017%22&limit=1).

Why it’s dangerous

The wrap contains fish, an allergen that was not listed on the product label. This means individuals with fish allergies could unknowingly consume the product and experience an allergic reaction.

Who’s affected

People with fish allergies are at risk of allergic reactions if they eat the recalled Everroast Chicken Caesar Wraps. The product is sold in clear flexible plastic packaging.

How to tell if you have this one

Check for Everroast Chicken Caesar Wraps with UPC 72036-95828 in clear flexible plastic packaging. The product was sold with all code dates.

  • Brand
    Harris Teeter
  • Product
    Everroast Chicken Caesar Wrap, UPC: 72036-95828, in clear flexible plastic
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC 72036-95828 on the packaging to identify the recalled Everroast Chicken Caesar Wrap.

Where it went and when

Where it was distributed

Distributed in 7 states and D.C..

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “DC, DE, FL, GA, MD, NC, SC, VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Delaware, District of Columbia, Florida, Georgia, Maryland, North Carolina, South Carolina, Virginia.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Jan 6, 201712. FDA classified it Class II: Jan 26, 201723. Published in FDA’s Enforcement Report: Feb 1, 201734. FDA terminated the recall: May 26, 201742017
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1367-2017 (January 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1367-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA