Illumina recalls NextSeq 550Dx instruments with specific Universal Copy Service software versions due to cybersecurity vulnerabilities. Affected units may have security risks.
Cybersecurity vulnerability concerning the software used for sequencing instruments.
Illumina is recalling NextSeq 550Dx instruments with certain software versions because of cybersecurity vulnerabilities. This could allow unauthorized access to the system, though the recall does not specify immediate harm to users.
The cybersecurity vulnerability in the Universal Copy Service software could allow unauthorized access to the instrument's data or system. This might lead to potential data breaches or system compromise if not addressed.
Users of NextSeq 550Dx instruments with Universal Copy Service software versions 1.4.2.927, 1.6.3.1423, or 2.7.2.4320 are affected. Laboratory personnel and researchers using these instruments are most at risk.
Check if your NextSeq 550Dx instrument has Universal Copy Service software version 1.4.2.927, 1.6.3.1423, or 2.7.2.4320. The instrument's unique identifier (UDI-DI) is (00)816270020125.
Identify your Universal Copy Service software version by checking the instrument's settings or documentation.
The recall addresses a cybersecurity vulnerability that could allow unauthorized access, but it does not specify immediate harm to users.
The recall does not provide specific action steps for affected users, so contact Illumina directly for guidance.
Check if your Universal Copy Service software version is 1.4.2.927, 1.6.3.1423, or 2.7.2.4320, and verify the instrument's UDI-DI number is (00)816270020125.
We’ve drafted a message you can send Illumina to request your refund or repair — edit it as you like.
Subject: Recall Z-1976-2023 — Illumina Illumina Hello, I own a Illumina that is covered by recall Z-1976-2023 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.
