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Stop using now Food recall · FDA · Published September 29, 2017

Hannaford Ham Salad Club Roll Recalled for Listeria Risk

Greencore USA recalls Hannaford Ham Salad Club Rolls (5.1 oz) due to possible Listeria monocytogenes contamination. Check your fridge.

🇺🇸 FDA recall #F-0072-2018FoodHannaford ›
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Recalling firmGreencore USA, LLC320 Commerce Park Rd · North Kingstown, RI 02852-8419
✎ GovInfoNow plain-language explainer

What happened, in plain English

Greencore USA, LLC is recalling Hannaford Ham Salad Club Rolls weighing 5.1 ounces because the product may be contaminated with Listeria monocytogenes. The recall covers items sold in Massachusetts, Rhode Island, Connecticut, Maine, Vermont, New Hampshire, and New York between September 28 and October 2. This is a Class I recall, indicating a serious health risk. Read more at govinfonow.com/recall/20394-hannaford-ham-salad-club-roll-recalled-for-listeria-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/20394-hannaford-ham-salad-club-roll-recalled-for-listeria-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-0072-2018

Cite this page

“Hannaford Ham Salad Club Roll Recalled for Listeria Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/20394-hannaford-ham-salad-club-roll-recalled-for-listeria-risk. Based on FDA recall #F-0072-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0072-2018%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacteria that can cause listeriosis, a serious infection. Infection can lead to fever, muscle aches, and gastrointestinal symptoms, and may spread to the nervous system causing headaches, stiff neck, or confusion. It can be fatal for high-risk groups.

Who’s affected

Consumers who purchased Hannaford Ham Salad Club Rolls (5.1 oz) in the Northeastern United States between September 28 and October 2 are likely affected. Individuals with weakened immune systems, pregnant women, older adults, and young children are at the highest risk for serious infection from Listeria.

How to tell if you have this one

Look for Hannaford Ham Salad Club Rolls in 5.1 oz packaging. Check the Best Buy Date on the label, which will be between 09/28 and 10/2. The product was distributed in Massachusetts, Rhode Island, Connecticut, Maine, Vermont, New Hampshire, and New York.

  • Brand
    Hannaford
  • Category
    Food
FDA recall event · 5 products

All 5 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    Massachusetts, Rhode Island, Connecticut, Maine, Vermont, New Hampshire and New York.
Recall numberProduct, codes & lotsQuantity
F-0068-2018(1) Walgreens NICE Egg Salad on White Bread, 6.1 oz (2) Turkey Hill Fresh Selects Egg salad on Homestyle Bread,4.7 oz (3)Target Egg salad on White Bread, 5.9 oz. (4) American Food and Vending Enza Choice Egg Salad on White Bread,4.7 oz Packaged in plastic wedge container.; Best Buy Date: Product 1-3: 9/29-10/1 Product 4: 10/12598 sandwiches
F-0069-2018(1)Turkey Hill Fresh Selects Ham salad on Homestyle Bread, 4.9 oz (2)American Food and Vending Enza Choice Ham Salad on White Bread, 4.7 oz Packaged in plastic wedge container.; Best Buy Date: (1) 9/29-10/1 (2)10/1316 sandwiches
F-0070-2018Hannaford Classic Seafood Stuffing, Plastic Tub, Net Wt. 10 oz; Best Buy Date: 10/2- 10/192658/10 oz. units
F-0071-2018Hannaford Egg Salad Club Roll 5.1 oz; Best Buy Date: 9/28-10/2653 cases ( 2 per case)
F-0072-2018Hannaford Ham Salad Club Roll, 5.1 oz; Best Buy Date: 09/28 - 10/2358 cases (2 per case)
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the Hannaford Ham Salad Club Roll if you have it at home due to the risk of Listeria contamination.

  2. Discard or return the item

    The record does not specify a specific remedy such as a refund or replacement, so consumers should discard the product or contact the retailer for assistance.

Where it went and when

Where it was distributed

Distributed in 7 states.

Alaska: not listedAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: yesCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Massachusetts, Rhode Island, Connecticut, Maine, Vermont, New Hampshire and New York.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Connecticut, Maine, Massachusetts, New Hampshire, New York, Rhode Island, Vermont.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Sep 29, 201712. FDA classified it Class I: Oct 27, 201723. Published in FDA’s Enforcement Report: Nov 8, 201734. FDA terminated the recall: Mar 27, 2018420172018
  1. Firm started the recall
  2. FDA classified it Class I
  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-0072-2018 (September 29, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0072-2018 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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