Oregon Potato Company recalls IQF 1/4" Yellow Onion Dice (item numbers 103364, 103381, 104831) due to potential Listeria monocytogenes contamination. Consumers should check product labels for lot numbers 6078-161B086.
IQF 1/4" Frozen Yellow Onion Dice is voluntarily recalled because it has the potential to be contaminated with Listeria monocytogenes.
Oregon Potato Company is recalling frozen yellow onion dice that may be contaminated with Listeria monocytogenes. This bacteria can cause serious illness, so affected products should be discarded to prevent foodborne illness.
Listeria monocytogenes is a bacteria that can cause serious foodborne illness, especially in pregnant women, newborns, the elderly, and those with weakened immune systems. The recall is due to potential contamination in the frozen onion dice.
Consumers who purchased the recalled frozen yellow onion dice from bulk cases with net weight 45 lbs. are affected. Those handling the product without proper food safety practices are at higher risk.
Check for item numbers 103364, 103381, or 104831 on bulk cases with a net weight of 45 lbs. Look for lot numbers 6078 through 161B086 on the packaging.
Immediately throw away any recalled frozen yellow onion dice with item numbers 103364, 103381, or 104831.
Lot numbers 6078, 6082, 161A068, 161A075, 161A076, 161A086, 161B068, 161B071, 161B074, 161B075, 161B076, 161B085, and 161B086.
Check the item number on the bulk case packaging. If it is 103364, 103381, or 104831, and the lot number is between 6078 and 161B086, it is recalled.
The recall does not provide a remedy; affected products should be discarded immediately.
We’ve drafted a message you can send Oregon Potato Company to request your refund or repair — edit it as you like.
Subject: Recall F-1938-2016 — Oregon Potato Company Oregon Potato Company Hello, I own a Oregon Potato Company that is covered by recall F-1938-2016 from Oregon Potato Company. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
