Cuson Sc2000 Ultrasound System - Mainframe (2016-03-08)

ACUSON SC2000 Ultrasound System Mainframe Recall Siemens is recalling the ACUSON SC2000 ultrasound system mainframe due to a potential software defect that could cause the device to shut down unexpectedly during patient examinations. This recall affects units distributed across Canada. The defect was classified as a Class I recall, indicating a serious safety concern.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-03-17

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0db9af2c-48fe-41c3-b068-df11856c996e