Illumina recalls NextSeq 550 Dx instruments with Local Run Manager software versions 1.3.1 to 3.0 due to cybersecurity vulnerability. Affected units include specific model numbers and UDI-DI codes listed in the recall notice.
cybersecurity vulnerability
Illumina has recalled its NextSeq 550 Dx DNA sequencers that run Local Run Manager software versions 1.3.1 to 3.0 due to a cybersecurity vulnerability. This could allow unauthorized access to the device's data. Users should check if their instrument is affected and follow the recall instructions.
The cybersecurity vulnerability in the Local Run Manager software could allow unauthorized access to the device's data. This risk exists if the software is not updated to a secure version, potentially exposing sensitive genetic information.
Users of Illumina NextSeq 550 Dx sequencers with Local Run Manager software versions 1.3.1 to 3.0 are affected. Researchers and labs using these instruments for genetic sequencing may be at risk of data breaches.
Check if your NextSeq 550 Dx instrument has Local Run Manager software version 1.3.1 to 3.0. Affected units are identified by specific model numbers and UDI-DI codes listed in the recall notice.
Verify your Local Run Manager software version by checking the instrument's settings or documentation. If it is version 1.3.1 to 3.0, it is affected.
Update to a secure software version by contacting Illumina directly for instructions on how to update the software.
Check if your instrument has Local Run Manager software version 1.3.1 to 3.0. Affected units are identified by specific model numbers and UDI-DI codes listed in the recall notice.
Contact Illumina directly for instructions on updating your Local Run Manager software to a secure version.
The vulnerability could allow unauthorized access to your device's data, potentially exposing sensitive genetic information.
We’ve drafted a message you can send Illumina to request your refund or repair — edit it as you like.
Subject: Recall Z-1260-2022 — Illumina Illumina Hello, I own a Illumina that is covered by recall Z-1260-2022 from Illumina. 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.
