Implantable defibrillator recalled for manufacturing defect causing device failure risk
Medtronic is recalling five implantable defibrillators due to a manufacturing defect where weld cracks caused devices to fail quality testing. The defective devices were identified during manufacturing and did not reach patients.
- Product
- Cobalt XT DR MRI SureScan, Model Number DDPA2D1, Implantable Cardioverter Defibrillator
- Category
- Medical Device
- Distribution
- Distributed nationwide