IQF 3/8" Yellow Onion Strip, Frozen, Item number 103331, bulk tote, net wt. 1150 lbs. IQF 3/8" Yellow Onion Strip, Frozen, item number 103368, bulk case, net wt. 40 lbs. Onion, Strips 3/8" 103369 40#, item number 103369, bulk case, net wt. 40 lbs. IQF 3/8" Yellow ORGANIC Onion Strip, Item number 103356, bulk tote, net wt. 1150 lbs.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    LOT numbers: 161A073; 161A080; 161A084; 161A085; 161B068; 161B073; 161B080; 161B084; 163A089.
  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:
Oregon Potato Company
Reason for Recall:
IQF 3/8" Frozen Yellow Onion Strip and IQF 3/8" Yellow ORGANIC Onion Strip are voluntarily recalled because it 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:

IQF 3/8" Yellow Onion Strip, Frozen, Item number 103331, bulk tote, net wt. 1150 lbs. IQF 3/8" Yellow Onion Strip, Frozen, item number 103368, bulk case, net wt. 40 lbs. Onion, Strips 3/8" 103369 40#, item number 103369, bulk case, net wt. 40 lbs. IQF 3/8" Yellow ORGANIC Onion Strip, Item number 103356, bulk tote, net wt. 1150 lbs.

Product Codes/Lot Numbers:

LOT numbers: 161A073; 161A080; 161A084; 161A085; 161B068; 161B073; 161B080; 161B084; 163A089.

Distribution:

Distributed in: AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ, OH, OR, TN, TX, UT, WA, WI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1939-2016

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