Fire-Roasted Corn & Black Bean Blend; Sold in 2 lb. containers. Brand Name: Jon-Lin¿ NatureSmart¿

Class I - Dangerous
Recalled: October 13, 2018 McCain Foods USA Other Foods

What Should You Do?

  1. Check if you have this product:
    All products shipped on or after January 1, 2016 Batch numbers: 1002015950 1002181334 1002229373 1002270376 1002309965 1002428675 1002530391 1002596743 1002666832 1002755315 1002820782 1001574724 1001611199 1001823843 1001877720 1001938394 1001968884 1001588449 1001732302
  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:
McCain Foods USA
Reason for Recall:
During an internal audit at the manufacturing location, it was discovered that finished product had been released on numerous occasions after receiving presumptive positive test results for Listeria monocytogenes and Salmonella; confirmation was not conducted.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Fire-Roasted Corn & Black Bean Blend; Sold in 2 lb. containers. Brand Name: Jon-Lin¿ NatureSmart¿

Product Codes/Lot Numbers:

All products shipped on or after January 1, 2016 Batch numbers: 1002015950 1002181334 1002229373 1002270376 1002309965 1002428675 1002530391 1002596743 1002666832 1002755315 1002820782 1001574724 1001611199 1001823843 1001877720 1001938394 1001968884 1001588449 1001732302

Distribution:

Distributed in: US

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0254-2019

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