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Lower risk Food recall · FDA · Published July 8, 2017

Sunneen Health Foods PB & J Parfait Recall: Missing Soy, Almonds, Coconut Allergens

Sunneen Health Foods recalls Whole Foods Market PB & J Parfaits (8 oz) due to misbranded product failing to list soy, almonds, and coconut allergens. Consumers should check labels for correct ingredients.

🇺🇸 FDA recall #F-3350-2017FoodSunneen Health Foods ›
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Recalling firmSunneen Health Foods, LLC375 W Greenleaf St · Allentown, PA 18102-1816
✎ GovInfoNow plain-language explainer

What happened, in plain English

Sunneen Health Foods is recalling Whole Foods Market PB & J Parfaits (8 oz) because they were mislabeled as PB & J when they actually contain vegan match cocoa. This means people with allergies to soy, almonds, or coconut could be at risk if they eat the product without knowing. Read more at govinfonow.com/recall/20670-sunneen-health-foods-pb-j-parfait-recall-missing-soy-almonds.

Source Summary by GovInfoNow · govinfonow.com/recall/20670-sunneen-health-foods-pb-j-parfait-recall-missing-soy-almonds · Updated October 8, 2026 · FDA enforcement record: FDA #F-3350-2017

Cite this page

“Sunneen Health Foods PB & J Parfait Recall: Missing Soy, Almonds, Coconut Allergens.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/20670-sunneen-health-foods-pb-j-parfait-recall-missing-soy-almonds. Based on FDA recall #F-3350-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3350-2017%22&limit=1).

Why it’s dangerous

The product was misbranded as a PB & J Parfait when it actually contains vegan match cocoa. This means the ingredient list did not properly list soy, almonds, and coconut allergens, which could cause allergic reactions in sensitive individuals.

Who’s affected

People who bought the Whole Foods Market PB & J Parfaits (8 oz) from stores that sell these products. Those with allergies to soy, almonds, or coconut are most at risk if they consumed the product without seeing the correct allergen labels.

How to tell if you have this one

Check for Whole Foods Market PB & J Parfaits (8 oz) with expiration date 7/13/17. The product was mislabeled as PB & J when it actually contains vegan match cocoa.

  • Brand
    Sunneen Health Foods
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the expiration date 7/13/17 on the label to confirm if it's the recalled item.

Where it went and when

Where it was distributed

Distributed in New Jersey and New York.

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: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: 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: “NJ, NY” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New Jersey, New York.

Recall timeline

FDA terminated this recall 7 months after the firm started it.

1. Firm started the recall: Jul 8, 201712. FDA classified it Class I: Aug 4, 201723. Published in FDA’s Enforcement Report: Aug 16, 201734. FDA terminated the recall: Jan 26, 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-3350-2017 (July 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3350-2017 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