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Stop using now Food recall · FDA · Published June 3, 2016

MaraNatha Sunflower Seed Butter Recalled for Listeria Risk

The Hain Celestial Group recalls MaraNatha All Natural Sunflower Seed Butter due to potential Listeria monocytogenes contamination. Check your UPC and use-by date.

🇺🇸 FDA recall #F-1845-2016FoodMaraNatha ›
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Recalling firmThe Hain Celestial Group, Inc. - Worldwide HQ1111 Marcus Ave · New Hyde Park, NY 11042-1221
✎ GovInfoNow plain-language explainer

What happened, in plain English

The Hain Celestial Group, Inc. is recalling MaraNatha All Natural Sunflower Seed Butter because a potential for Listeria monocytogenes contamination was verified by the sunflower seed raw material supplier. This Class I recall affects 14,533 cases of the 12 oz product distributed across the United States and available online. Consumers should check their pantry for affected items immediately. Read more at govinfonow.com/recall/24149-maranatha-sunflower-seed-butter-recalled-for-listeria-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/24149-maranatha-sunflower-seed-butter-recalled-for-listeria-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-1845-2016

Cite this page

“MaraNatha Sunflower Seed Butter Recalled for Listeria Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/24149-maranatha-sunflower-seed-butter-recalled-for-listeria-risk. Based on FDA recall #F-1845-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1845-2016%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacterium that can cause serious infections in humans. Ingestion of contaminated food can lead to severe illness, especially for vulnerable populations, even if the product looks and smells normal.

Who’s affected

Consumers in the United States who purchased MaraNatha All Natural Sunflower Seed Butter, particularly those who bought it between July 28, 2016, and December 5, 2016. Individuals with weakened immune systems, pregnant women, the elderly, and young children are at higher risk for serious infection from Listeria.

How to tell if you have this one

Look for MaraNatha All Natural Sunflower Seed Butter in 12 oz (340g) jars with UPC code 0 51651-09367 5. Check the 'Use By' date on the label, which will fall between July 28, 2016 (28JUL16) and December 5, 2016 (05DEC16).

  • Brand
    MaraNatha
  • Product
    MaraNatha¿ All Natural Sunflower Seed Butter, NET WT 12 OZ (340g)., UPC 0 51651-09367 5
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled sunflower seed butter if you have it in your home.

  2. Check the UPC and date

    Verify that your jar has UPC 0 51651-09367 5 and a use-by date between 28JUL16 and 05DEC16.

  3. Dispose of the product

    Discard any affected jars to prevent potential illness from Listeria contamination.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Products were distributed across the United States. The products also were available for purchase on the internet.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2 years after the firm started it.

1. Firm started the recall: Jun 3, 201612. FDA classified it Class I: Jul 28, 201623. Published in FDA’s Enforcement Report: Aug 3, 201634. FDA terminated the recall: Jun 15, 2018420162018
  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-1845-2016 (June 3, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1845-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 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