medical Class II Updated 2024-01-17

Siemens Medical Solutions USA, Inc recalls Sensis Vibe Hemo

Recalled Product

Sensis Vibe Hemo


Hazard / Issue

The possibility of the Sensis documentation functionality application to crash.

Issued by

FDA

Affected States: CA, CT, FL
Lot/Code Info: Model No. 11007641; UDI-DI 04056869010199; Serial No. 18009, 106245, 18016, 18014, 18011, 18010, 19001, 106244, 18015.
View official government recall

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