IQF Yellow Onion Dice (Oregon Potato) – Listeria Risk (2016)
Class I: A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
705000 IQF 3/8" Dice Yellow Onion, item number 101472, bulk tote, net wt. 1250 lbs. IQF 3/8" Yellow Onion Dice, item number 103330, 103341, bulk cases, net wt. 20 lbs. IQF 3/8" Yellow Onion Dice, item numbers 101578, 104147, and 104193, bulk cases, net wt. 45 lbs. IQF 3/8" Yellow Onion Dice, item number 101578, bulk container
Brand
Oregon Potato Company
Lot Codes / Batch Numbers
LOT numbers: 161A070, 161A071, 161A072, 161A073, 161A074, 161A075, 161A076, 161A079, 161A080, 161A081, 161A082, 161A083, 161A084, 161A089, 161B069, 161B070, 161B071, 161B072, 161B074, 161B079, 161B081, 161B083, 161B088.
Products Sold
LOT numbers: 161A070, 161A071, 161A072, 161A073, 161A074, 161A075, 161A076, 161A079, 161A080, 161A081, 161A082, 161A083, 161A084, 161A089, 161B069, 161B070, 161B071, 161B072, 161B074, 161B079, 161B081, 161B083, 161B088.
Oregon Potato Company is recalling 705000 IQF 3/8" Dice Yellow Onion, item number 101472, bulk tote, net wt. 1250 lbs. IQF 3/8" Yell due to 3/8" Frozen Yellow Onion Dice was voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
3/8" Frozen Yellow Onion Dice was voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, CA, CO, GA, IN, KY, LA, MA, MI, NJ, OH, OR, TN, TX, UT, WA, WI
Page updated: Jan 6, 2026