Oregon Potato Company recalls IQF frozen yellow onion dice (item 102654) due to potential Listeria monocytogenes contamination. Consumers should check lot numbers 161A075-161B076 for affected products.
1/4 x 1/4 Frozen Yellow Onion Dice was 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 consumers should stop using the product immediately.
Listeria monocytogenes is a bacteria that can cause serious infections, especially in pregnant women, newborns, and people with weakened immune systems. Contaminated food can lead to severe illness or death if consumed.
Anyone who purchased the recalled frozen yellow onion dice from bulk cases with lot numbers 161A075 through 161B076. People with weakened immune systems are at higher risk for severe illness.
Check for bulk cases labeled 'IQF 1/4 x 1/4 Yellow Onion Dice' with item number 102654 or 103205. Look for lot numbers 161A075, 161A076, 161B068, 161B075, or 161B076 on the packaging.
Immediately discard any recalled frozen yellow onion dice with lot numbers 161A075 through 161B076.
Lot numbers 161A075, 161A076, 161B068, 161B075, and 161B076.
Check the lot number on the packaging; affected products have lot numbers 161A075 through 161B076.
Yes, Listeria monocytogenes can cause serious illness, especially in pregnant women, newborns, and people with weakened immune systems.
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-1945-2016 — Oregon Potato Company Oregon Potato Company Hello, I own a Oregon Potato Company that is covered by recall F-1945-2016 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.
