Mammotrak Diagnostic Coil 1.5T Recalled Due to Patient Safety Concern
Philips is recalling 5,231 Mammotrak Diagnostic Coil 1.5T units nationwide because of a potential patient safety issue during MRI scans. The FDA has classified this as a Class II recall.
- Product
- Mammotrak Diagnostic Coil 1.5T
- Category
- Medical Device
- Distribution
- Distributed nationwide