🔍 RecallPedia

ROASTED & UNSALTED SUNFLOWER KERNELS sold under the following labels: 1) ROASTED & UNSALTED SUNFLOWER KERNELS, 10.25 oz, shipped 12 packs per case, 2) Tops square tub ROASTED & UNSALTED SUNFLOWER KERNELS, 10.25 oz, shipped 12 packs per case, 3) EARTH FARE ROASTED & UNSALTED SUNFLOWER KERNELS, NET WT 16 OZ (1 LB) 453g, shipped 6 per case

Class I - Dangerous
Recalled: May 23, 2016 First Source Other Foods

What Should You Do?

  1. Check if you have this product:
    1) BEST BY 03/23/17, 3/30/17, & 5/3/17 2) BEST By 3/30/17 & 5/3/17 3) BEST By 06/04/16 - 05/31/17
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
First Source Llc
Reason for Recall:
Product has the potential to be contaminated with Listeria monocytogenes
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

ROASTED & UNSALTED SUNFLOWER KERNELS sold under the following labels: 1) ROASTED & UNSALTED SUNFLOWER KERNELS, 10.25 oz, shipped 12 packs per case, 2) Tops square tub ROASTED & UNSALTED SUNFLOWER KERNELS, 10.25 oz, shipped 12 packs per case, 3) EARTH FARE ROASTED & UNSALTED SUNFLOWER KERNELS, NET WT 16 OZ (1 LB) 453g, shipped 6 per case

Product Codes/Lot Numbers:

1) BEST BY 03/23/17, 3/30/17, & 5/3/17 2) BEST By 3/30/17 & 5/3/17 3) BEST By 06/04/16 - 05/31/17

Distribution:

Distributed in: IN, LA, MA, MD, MI, NJ, NY, PA, VA, WV, SC

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0697-2017

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