Cuson Sc2000 Prime Ultrasound System - Mainframe (2018-01-31)
Recall Summary Siemens is recalling the ACUSON SC2000 PRIME Ultrasound System Mainframe across Canada due to a defect that could affect its performance. This recall applies to ultrasound systems distributed in Canada. The FDA has classified this as a Class I recall, indicating a serious issue with the device.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-02-16
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/e2ee7936-578f-4d15-97ca-b77dc0f51734