Medtronic Recalls KYPHON Directional Bone Filler Devices Due to Alignment Defect
Medtronic is recalling KYPHON Directional Bone Filler Devices because the directional arrow may not align with the opening, potentially causing cement to be placed in an unintended direction.
- Product
- KYPHON(R) Directional Bone Filler Device, Size: 3, REF F04C, Rx Only, STERILE R.
- Category
- Medical Device
- Distribution
- 0 states