Siemens recalls Sensis Vibe systems with VD15B software that may crash when adding certain reporting events. Affected units include specific model numbers for cardiac and interventional radiology procedures.
If the Sensis documentation functionality is used during adding of once-per-study reporting events (e.g., Type 1 events, as further defined in the administrator manual), the possibility exists that the application could crash.
Siemens is recalling Sensis Vibe systems with software version VD1:5B that may crash when adding specific reporting events. This could disrupt medical procedures and requires immediate attention to prevent potential errors in patient care.
The system may crash when adding certain reporting events, such as Type 1 events, which are used in medical procedures. This could lead to errors in patient data or procedure documentation, but does not pose a direct physical risk to users.
Healthcare providers using Sensis Vibe systems with software version VD15B for cardiac or interventional radiology procedures are most at risk. Patients undergoing these procedures may be affected if the system crashes during critical reporting events.
Check for software version VD15B on Sensis Vibe systems paired with AXIOM Sensis Post Processing Workstation. Affected units have model number 6648161 and serial numbers 18904 or 18906.
Verify the software version on your Sensis Vibe system to see if it is VD15B.
The recall indicates a potential for system crashes during specific reporting events, but it does not pose a direct physical risk to users. This is considered low risk.
Check your software version. If it is VD15B, contact Siemens for guidance on next steps.
Affected units have model number 6648161 and serial numbers 18904 or 18906. Check your software version to see if it is VD15B.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2440-2024 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2440-2024 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.
