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Lower risk Food recall · FDA · Published May 30, 2017

ASK Foods Greek Pasta Salad Recall: May Contain Undeclared Milk

ASK Foods recalls Greek Pasta Salad (10 oz) due to possible undeclared milk. Consumers should check for incorrect nutrition labels from another product.

🇺🇸 FDA recall #F-2416-2017FoodASK Foods ›
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Recalling firmASK Foods Inc77 N Hetrick Ave · Palmyra, PA 17078-1501
✎ GovInfoNow plain-language explainer

What happened, in plain English

ASK Foods is recalling a specific lot of Greek Pasta Salad because it may contain milk that wasn't listed on the label. This could affect people with dairy allergies or sensitivities. Read more at govinfonow.com/recall/21150-ask-foods-greek-pasta-salad-recall-may-contain-undeclared-milk.

Source Summary by GovInfoNow · govinfonow.com/recall/21150-ask-foods-greek-pasta-salad-recall-may-contain-undeclared-milk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2416-2017

Cite this page

“ASK Foods Greek Pasta Salad Recall: May Contain Undeclared Milk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21150-ask-foods-greek-pasta-salad-recall-may-contain-undeclared-milk. Based on FDA recall #F-2416-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2416-2017%22&limit=1).

Why it’s dangerous

The product may contain milk that wasn't declared on the label. This happens because the nutrition label from a different product (Taste of Inspirations Classic Red Skin Potato Salad) was mistakenly used on the Greek Pasta Salad packaging.

Who’s affected

People who purchased the recalled Greek Pasta Salad from Hannaford Supermarkets are affected. Those with dairy allergies or sensitivities are at higher risk.

How to tell if you have this one

Check for the product code 3649-1 on the packaging. The recall involves Greek Pasta Salad (10 oz) sold by Hannaford Supermarkets in the US.

  • Brand
    ASK Foods
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Packaging

    Look for the product code 3649-1 on the packaging to identify if it's part of the recall.

Where it went and when

Where it was distributed

Distributed in 5 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: not listedRIMassachusetts: yesMAOregon: 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: 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: “MA, ME, NH, NY and VT” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maine, Massachusetts, New Hampshire, New York, Vermont.

Recall timeline

FDA terminated this recall 8 months after the firm started it.

1. Firm started the recall: May 30, 201712. FDA classified it Class I: Jun 30, 201723. Published in FDA’s Enforcement Report: Jul 12, 201734. FDA terminated the recall: Feb 7, 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.

✎ GovInfoNow

Questions people ask

Is there a risk of serious injury?

No, the recall is for people with dairy allergies or sensitivities, not a physical safety hazard.

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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-2416-2017 (May 30, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2416-2017 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