Oscor SafeSheath ULTRALITE 10F Recalled for Potential Open Sterile Seal
Oscor, Inc. is recalling 500 units of the AngioDynamics SafeSheath ULTRALITE 10F due to a potential open seal on the sterile product.
- Product
- AngioDynamics SafeSheath ULTRALITE 10F, Model Number VI10 - Product Usage: intended for the introduction of various types of pacing leads and catheters.
- Category
- Medical Device
- Distribution
- Distributed nationwide