Siemens recalls Sensis Vibe systems with specific software version VD15B that may crash when adding certain reporting events. Affected units include specific serial numbers for cardiac and interventional radiology applications.
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 VD15B that may crash when adding specific reporting events. This could disrupt medical procedures during cardiac or interventional radiology studies. Affected units have unique serial numbers listed in the recall notice.
The software may crash when adding certain reporting events, such as Type 1 events, during medical procedures. This could disrupt the system's functionality but does not indicate a risk of injury or serious harm.
Healthcare professionals using Siemens Sensis Vibe systems for cardiac or interventional radiology procedures may be affected. Those with specific serial numbers listed in the recall are most at risk.
Check if your Sensis Vibe system has software version VD15B and the model number 10765502. Affected units have specific serial numbers: 18023, 18022, 18020, 18021, 18019, 18025, 18017.
Verify your Sensis Vibe system has software version VD15B and model number 10765502.
The affected software version is VD15B.
The system may crash when adding certain reporting events, such as Type 1 events, which could disrupt medical procedures.
Affected serial numbers are 18023, 18022, 18020, 18021, 18019, 18025, and 18017.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-2439-2024 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-2439-2024 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.
