Siemens Sensis Vibe Hemo Device May Crash - Recall Notice
Siemens recalls Sensis Vibe Hemo devices with specific serial numbers due to potential documentation crashes. Affected units may experience application failures; contact for remedy.
Lower-risk recall
The possibility of the Sensis documentation functionality application to crash.
Contact the company
What happened, in plain English
Siemens is recalling certain Sensis Vibe Hemo devices because their documentation functionality might crash. This could disrupt medical records and affect patient care. The recall applies to specific serial numbers listed in the notice. Read more at govinfonow.com/recall/56727-siemens-sensis-vibe-hemo-device-may-crash-recall-notice.
Source Summary by GovInfoNow · govinfonow.com/recall/56727-siemens-sensis-vibe-hemo-device-may-crash-recall-notice · Updated August 18, 2026 · FDA enforcement record: FDA #Z-0683-2024
Cite this page
“Siemens Sensis Vibe Hemo Device May Crash - Recall Notice.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/56727-siemens-sensis-vibe-hemo-device-may-crash-recall-notice. Based on FDA recall #Z-0683-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0683-2024%22&limit=1).
Why it’s dangerous
The device's documentation functionality might crash, causing medical records to become unavailable. This could lead to disruptions in patient care if the system fails during critical tasks. However, the crash is not expected to cause physical harm.
Who’s affected
Healthcare providers using the Sensis Vibe Hemo device with the listed serial numbers are most at risk. Patients using the device may also be affected if their medical records are disrupted.
How to tell if you have this one
Check the serial number on your device's label. Affected units have serial numbers: 18009, 106245, 18016, 18014, 18011, 18010, 19001, 106244, 18015.
- Brand
Siemens- Category
Medical device
What to do — step by step
Check Device Serial Number
Look for the serial number on your device's label to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “Domestic: CA, CT, & FL.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Connecticut, Florida.
Recall timeline
FDA published this recall 49 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0683-2024 (November 29, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0683-2024 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.