Synaptive Medical

5 recalls Categories: Infusion Pumps, Other Medical Devices, Surgical Instruments
Class I - Dangerous

A software defect negatively affects the quality of images taken during diagnostic imaging (mammograms) which may result in misdiagnosis.

Feb 26, 2020 Other Medical Devices View Details →

This recall has been initiated due to a software defect found in the Guide System software when used with NICO BrainPath ports under certain circumstances. When one trajectory is set with a blue port and another trajectory is set with a gold port, the software defect is triggered when the user switches between these trajectories during a surgical procedure.

Oct 9, 2018 Infusion Pumps Nationwide View Details →

Out of tolerance for radio frequency emissions. At the 150-1000MHz frequency, the testing indicated the BrightMatter Navigation system was up to 20dB uV/meter higher than the applicable IEC 60601-1-2:2007 (Ed3.0) standard specification.

Dec 4, 2015 Surgical Instruments View Details →