Ivenix Infusion System Devices Recalled for Alarm Sequencing Defect
The Ivenix Infusion System may malfunction where an occlusion alarm is immediately followed by a pump problem alarm, potentially delaying proper identification of the issue. FDA is recalling 1,335 affected devices.
- Product
- Ivenix Infusion System (IIS)
- Category
- Medical Device
- Distribution
- Distributed nationwide