Class II
Medical Device Recall: Sensis Vibe Hemo
Siemens Medical Solutions USA, Inc · November 29, 2023
Reason for Recall
The possibility of the Sensis documentation functionality application to crash.
Distribution
Domestic: CA, CT, & FL.
States Affected
CA, CT, FL
Quantity Affected
331 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0683-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.