Saut¿ed Julienne Onion Strips With Canola Caramel; 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: 1002371779 1002373359 1001587731 1002058202 1002085830 1001628771 1001701451 1001754195 1001812995 1001851116 1002162007 1002189078 1002404837 1002427345 1002574046 1002587601 1002647589 1002715213 1002792707
  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:

Saut¿ed Julienne Onion Strips With Canola Caramel; Sold in 20 lb. containers. Brand Name: Jon-Lin¿

Product Codes/Lot Numbers:

All products shipped on or after January 1, 2016 Batch numbers: 1002371779 1002373359 1001587731 1002058202 1002085830 1001628771 1001701451 1001754195 1001812995 1001851116 1002162007 1002189078 1002404837 1002427345 1002574046 1002587601 1002647589 1002715213 1002792707

Distribution:

Distributed in: US

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0239-2019

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