Z-0683-2024 Class II Ongoing

Recalled by Siemens Medical Solutions USA, Inc — Malvern, PA

Recall Details

Product Type
Devices
Report Date
January 17, 2024
Initiation Date
November 29, 2023
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
331 units

Product Description

Sensis Vibe Hemo

Reason for Recall

The possibility of the Sensis documentation functionality application to crash.

Distribution Pattern

Domestic: CA, CT, & FL.

Code Information

Model No. 11007641; UDI-DI 04056869010199; Serial No. 18009, 106245, 18016, 18014, 18011, 18010, 19001, 106244, 18015.