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 - DangerousWhat Should You Do?
- Check if you have this product: LOT numbers: 161A073; 161A080; 161A084; 161A085; 161B068; 161B073; 161B080; 161B084; 163A089.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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.govFDA Recall Number: F-1939-2016
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