Illumina recalls MiSeq Dx instruments with software versions 1.3.1 to 3.0 due to a cybersecurity vulnerability. Affected models include DX-410-1001, 15036706, and 20014053. No remedy is specified in the recall notice.
cybersecurity vulnerability
Illumina is recalling MiSeq Dx instruments with software versions 1.3.1 to 3.0 due to a cybersecurity vulnerability. This affects specific model numbers and UDI-DI codes. The recall does not include a remedy or action steps.
The recall mentions a cybersecurity vulnerability but does not specify how it could lead to harm. Without details on the vulnerability's impact or potential risks, the danger level cannot be assessed.
Users of Illumina MiSeq Dx instruments with software versions 1.3.1 to 3.0 are affected. The risk is unclear without a specified remedy or hazard details.
Check if your MiSeq Dx instrument has software versions 1.3.1 to 3.0. Affected models include DX-410-1001, 15036706, and 20014053. UDI-DI codes listed in the recall include a long list of identifiers starting with M70 and C70.
Verify your MiSeq Dx instrument's software version. If it is between 1.3.1 and 3.0, it is affected.
The recall notice does not specify any remedy or action steps for this cybersecurity vulnerability.
Check if your instrument has software versions 1.3.1 to 3.0. Affected models include DX-410-1001, 15036706, and 20014053. UDI-DI codes listed in the recall include a long list of identifiers starting with M70 and C70.
The recall does not specify any action steps. You should contact Illumina directly for further guidance.
We’ve drafted a message you can send Illumina to request your refund or repair — edit it as you like.
Subject: Recall Z-1259-2022 — Illumina Illumina Hello, I own a Illumina that is covered by recall Z-1259-2022 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.
