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CriticalFDAfda-F-1665-2016LISTERIA

Quaker Quinoa Granola Bars, Chocolate Nut Medley packaged in a multi colored box with brown lettering. 5, 1.23 oz bars per box.

⚠ 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.

Units Affected
470
Recall Date
May 16, 2016
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1665-2016.

Sunflower kernels used in Quinoa bars are contaminated with Listeria Monocytogenes.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1665-2016.

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 Quaker Oats Company 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-1665-2016.

The Quaker Oats Company

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 Quaker Oats Company Recall FAQ

The Quaker Oats Company is the subject of a bakery & grains safety report: Quaker Quinoa Granola Bars, Chocolate Nut Medley packaged in a multi colored box with brown lettering. 5, 1.23 oz bars per box.. The notice was published on May 16, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 470 units are potentially affected.