Okami brand 8-piece Salmon Philly Roll (SKU 28113) with date codes from November 22, 2019 to December 6, 2019 may contain Listeria monocytogenes. Consumers should check their products and contact the manufacturer for guidance.
RTE products potentially contaminated with Listeria monocytogenes.
Okami brand 8-piece Salmon Philly Roll (SKU 28113) with date codes from November 22, 2019 to December 6, 2019 is recalled due to potential Listeria monocytogenes contamination. This bacteria can cause serious illness, especially in pregnant women, newborns, and the elderly.
Listeria monocytogenes is a bacteria that can cause serious infections in vulnerable populations. It can lead to miscarriages, stillbirths, sepsis, and meningitis in newborns, and can cause severe illness in the elderly and those with compromised immune systems.
Pregnant women, newborns, the elderly, and those with weakened immune systems are at higher risk from Listeria monocytogenes. Anyone who purchased the Okami brand 8-piece Salmon Philly Roll with date codes between November 22, 2019 and December 6, 2019 is likely affected.
Check for the Okami brand 8-piece Salmon Philly Roll with SKU 28113. The date code on the package should be between November 22, 2019 and December 6, 2019.
Look for the date code on the package, which should be between November 22, 2019 and December 6, 2019.
The recall record states that the product may be contaminated with Listeria monocytogenes, so it is not safe to eat.
Pregnant women, newborns, the elderly, and those with weakened immune systems are at higher risk from Listeria monocytogenes.
Check the date code on the package; if it falls between November 22, 2019 and December 6, 2019, the product is recalled.
We’ve drafted a message you can send Okami to request your refund or repair — edit it as you like.
Subject: Recall F-0429-2020 — Okami Okami Hello, I own a Okami that is covered by recall F-0429-2020 from Okami. 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.
