Karl Storz Ureteroscope Recalled for Unapproved Reprocessing Instructions
Karl Storz is recalling 180 ureteroscopes due to instructions for use containing reprocessing procedures that have not been reviewed or approved by the FDA.
- Product
- KARL STORZ - ENDOSKOPE, REF: 27002K, Ureteroscope, 9.5 Fr., 6¿, 34 cm, NON STERILE, RxONLY, CE 0123
- Category
- Medical Device
- Distribution
- Distributed nationwide