Fire Roasted Yellow Pepper Strips; Sold in 20 lb. containers. Brand Name: Jon-Lin¿

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: 1001893940 1002152263 1002180438 1002222384 1002235523 1002266084 1002278122 1002326661 1002347073 1002349933 1002360519 1002497592 1002505956 1002545797 1002617135 1002656863 1002715206 1002737971 1002767063 1002820783 1001922126
  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 Yellow Pepper Strips; Sold in 20 lb. containers. Brand Name: Jon-Lin¿

Product Codes/Lot Numbers:

All products shipped on or after January 1, 2016 Batch numbers: 1001893940 1002152263 1002180438 1002222384 1002235523 1002266084 1002278122 1002326661 1002347073 1002349933 1002360519 1002497592 1002505956 1002545797 1002617135 1002656863 1002715206 1002737971 1002767063 1002820783 1001922126

Distribution:

Distributed in: US

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0253-2019

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