Diagnostic Imaging Systems Missing FDA Certification Label
Philips North America is recalling 25 ProxiDiagnost N90 R.1.0 and CombiDiagnost R90 diagnostic imaging systems distributed nationwide because they are missing an FDA-required certification label.
- Product
- ProxiDiagnost N90 R.1.0
- Category
- Medical Device
- Distribution
- Distributed nationwide