Product Safety Recalls

Product Recall Tracker

Siemens Medical Solutions USA, Inc Recall 93637

Description: Sensis Vibe Hemo

Siemens Medical Solutions USA, Inc Recall 93637 Information

Mandated?Voluntary: Firm initiated
Recall NumberZ-0683-2024
Event ID93637
Event DescriptionSensis Vibe Hemo
Product TypeDevices
DistributionDomestic: CA, CT, & FL.
Quantity331 units
Recall ReasonThe possibility of the Sensis documentation functionality application to crash.
Device Classification20240117
Device Code InfoModel No. 11007641; UDI-DI 04056869010199; Serial No. 18009, 106245, 18016, 18014, 18011, 18010, 19001, 106244, 18015.
Center Classification Date20240109
Recall Initiation Date20231129
Recalling FirmSiemens Medical Solutions USA, Inc
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied. is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.