Bk3000/3500, Bk5000 And Bkactiv Ultrasound Systems
Recall Summary BK3000/3500, BK5000, and BKactiv Ultrasound Systems are being recalled across Canada due to a performance issue. This recall affects ultrasound equipment used in medical settings. The FDA has classified this as a Class I recall, indicating a serious concern with how the devices function.
- Product
- Bk3000/3500, Bk5000 and Bkactiv Ultrasound Systems
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-09-19
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/46e33911-3960-4990-88ad-85f6a2cebffc