Siemens recalls Sensis Vibe Combo with software version VD12A due to potential communication disconnect during first patient exam or after inactivity, risking no vital signs. Affected units have specific serial numbers.
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 Vibe Combo devices with software version VD12A because they may disconnect from the system during the first patient exam of the day or after extended inactivity, leading to unavailable vital signs. This could impact patient safety during critical medical procedures.
The 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, potentially delaying critical medical interventions.
Healthcare professionals using the Sensis Vibe Combo for hemodynamic catheterizations or electrophysiology studies are most at risk. Patients undergoing procedures with this device may experience interrupted vital sign monitoring.
Check for serial numbers listed: 123021, 123055, 123056, 123058, 122042, 123004, 122006, 122026, 122029, 123047, 123053, 122011, 121014. The device has software version VD12A for hemodynamic catheterizations and electrophysiology studies.
Verify the software version on your Sensis Vibe Combo device; affected units have version VD12A.
Reach out to Siemens Medical Solutions USA, Inc for guidance on next steps if your device is affected.
The recalled software version is VD12A.
Check for serial numbers listed: 123021, 123055, 123056, 123058, 122042, 123004, 122006, 122026, 122029, 123047, 123053, 122011, 121014.
The recall record does not specify a fix or remedy.
We’ve drafted a message you can send Siemens to request your refund or repair — edit it as you like.
Subject: Recall Z-1426-2022 — Siemens Siemens Hello, I own a Siemens that is covered by recall Z-1426-2022 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.
