Philips dS Breast MRI System Recalled for Patient Safety Hazard
Philips dS Breast 16ch 3.0T MRI systems are being recalled due to a potential safety issue that could harm patients during medical scans. The FDA-mandated Class II recall affects 5,231 units distributed nationwide.
- Product
- dS Breast 16ch 3.0T
- Category
- Medical Device
- Distribution
- Distributed nationwide