Siemens recalls Syngo.plaza software VB10A model numbers 10863171-10863173 due to potential patient misdiagnosis from incorrect study date formats and legacy presentation states. Affected healthcare facilities should contact Siemens for remediation.
Software upgrade to correct format of study dates and issues with Legacy Presentation States (annotations) in order to prevent potential patient misdiagnosis.
Siemens is recalling Syngo.plaza software versions VB10A with specific model numbers to prevent potential patient misdiagnosis caused by incorrect study date formats and issues with legacy presentation states. This recall affects healthcare facilities using these software versions for medical imaging systems.
The software has issues with study date formats and legacy presentation states that could lead to incorrect medical images being displayed. This might cause misdiagnosis if healthcare providers rely on the software for accurate patient imaging data.
Healthcare facilities using Siemens Syngo.plaza software VB10A model numbers 10863171, 10863172, or 10863173 are most at risk. These software versions are used in medical imaging systems for patient diagnosis and treatment planning.
Check if your Siemens Syngo.plaza software is version VB10A with model numbers 10863171, 10863172, or 10863173. These model numbers are associated with the affected software versions used in medical imaging systems.
Reach out to Siemens Medical Solutions USA, Inc for guidance on the recall and remediation steps for affected software versions.
Siemens Syngo.plaza software VB10A model numbers 10863171, 10863172, and 10863173.
The software has issues with study date formats and legacy presentation states that could lead to potential patient misdiagnosis.
Check your Siemens Syngo.plaza software model numbers to see if they are 10863171, 10863172, or 10863173.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1699-2018 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1699-2018 from Siemens. 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.
