Siemens recalls Sensis software version VD12A for potential disconnect during first patient exam or after inactivity, risking no vital signs. Affected units have specific serial numbers and model.
Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of its communication during the first patient examination of the day or after a longer period of inactivity to the Sensis Vibe system resulting in no vital signs being available.
Siemens is recalling Sensis software version VD12A due to a risk of communication disconnect during the first patient exam or after extended inactivity, which could lead to no vital signs being available. This affects specific medical devices used in cardiac and interventional radiology procedures.
The ComboBox feature in Sensis software version VD12A may disconnect communication with the Sensis Vibe system during the first patient examination of the day or after extended inactivity. This can result in no vital signs being available to the healthcare provider.
Healthcare providers using Sensis software version VD12A for hemodynamic catheterizations or electrophysiology studies are most at risk. The affected units have specific serial numbers and model.
Check for serial numbers 61331 or 60015 and model number 10764561. The software version VD12A is also part of the affected product.
Verify the software version on your Sensis device; if it is VD12A, it is affected.
The recalled software version is VD12A.
The communication may disconnect during the first patient examination of the day or after extended inactivity, resulting in no vital signs being available.
Check for serial numbers 61331 or 60015 and model number 10764561.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1425-2022 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1425-2022 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.
