Flexiva Pulse ID Laser Fiber Recalled for Potential Burn Hazard
Boston Scientific recalls Flexiva Pulse ID laser fibers used in urological procedures due to a manufacturing defect that may cause connector overheating and burns. The recall affects 205 units distributed in the US and Canada.
- Product
- Flexiva Pulse ID-intended to be used as a device that transmits Ho:YAG laser energy from cleared laser consoles to urological anatomy (Box of 5)UPN: M006L8406911
- Category
- Medical Device
- Distribution
- Distributed nationwide