Fire Roasted Green Pepper Strips ; 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: 1001552707 1001631796 1001669170 1002085832 1002209593 1002232240 1002307305 1002369497 1002454429 1002517048 1002611498 1002695644 1002747066 1002792708 1001695814 1001767570 1001835536 1001931257 1001982359
  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 Green Pepper Strips ; 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: 1001552707 1001631796 1001669170 1002085832 1002209593 1002232240 1002307305 1002369497 1002454429 1002517048 1002611498 1002695644 1002747066 1002792708 1001695814 1001767570 1001835536 1001931257 1001982359

Distribution:

Distributed in: US

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0251-2019

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