Ventana He 600 System (2019-10-30)
Ventana HE 600 System Recall The Ventana HE 600 System, a medical device used in laboratories, is being recalled across Canada. The device has a defect that poses a risk to patient safety or test accuracy. This recall affects healthcare facilities and laboratories that use this system.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-11-15
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/94f9fbc8-08bd-4f86-b829-548fcff0e3f7