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Siemens Medical Solutions USA, Inc recalls Sensis Vibe Hemo
Recalled January 17, 2024 · FDA recall Z-0683-2024 · Siemens Medical Solutions USA
Hazard
The possibility of the Sensis documentation functionality application to crash. · FDA Class II
Units
331 units
Sold at
Domestic: CA, CT, & FL.
Description
The possibility of the Sensis documentation functionality application to crash.
Product
Sensis Vibe Hemo
Manufacturer(s)
Siemens Medical Solutions USA, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →