Ngiojet Ultra 5000a Console
Angiojet Ultra 5000a Console Recall Summary The Angiojet Ultra 5000a Console, a medical device used in hospitals and clinics, is being recalled across Canada. The recall was issued due to a Class I safety concern, which is the most serious classification. This recall affects healthcare facilities and patients who may have received treatment using this device.
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-03-10
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/768552b3-652e-4de5-9894-459e2ff03b2d