Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 13–24 of 56 recalls
Due to a software implementation error that allowed instruments arms failing an important diagnostic test to remain in clinical use.…
Due to probe bags that may have a compromised or incomplete sterile pouch seal.
Access Port System tray may develop cracks potentially resulting in a sterility breach.
Surgical system Error 23062 due to connector1) Partially damaged "Potential problem with ergonomics: Disable - Retry " or 2) Failed "Disable Ergonomics: Viewer, headrest, armrest, and pedal tray position cannot be adjust…
Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed
Due to an increase in complaints for pitch cable failures related to forceps and small Graptor instruments
Due to an increase in complaints for pitch cable failures related to forceps and small Graptor instruments
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.