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CriticalFDAfda-F-1845-2016LISTERIA

MaraNatha¿ All Natural Sunflower Seed Butter, NET WT 12 OZ (340g)., UPC 0 51651-09367 5

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
14,533
Recall Date
June 3, 2016
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1845-2016.

A potential for Listeria monocytogenes contamination was verified by the sunflower seed raw material supplier.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1845-2016.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact The Hain Celestial Group, Inc. - Worldwide Hq or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1845-2016.

The Hain Celestial Group, Inc. - Worldwide HQ

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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The Hain Celestial Group, Inc. - Worldwide Hq Recall FAQ

The Hain Celestial Group, Inc. - Worldwide Hq is the subject of a dairy safety report: MaraNatha¿ All Natural Sunflower Seed Butter, NET WT 12 OZ (340g)., UPC 0 51651-09367 5. The notice was published on June 3, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 14,533 units are potentially affected.