Every recall we track for Remote Diagnostic Technologies Ltd. — 12 in all — plus the complaints and injury reports the public filed about them.
Remote Diagnostic Technologies Ltd. - Remote Diagnostic Technologies Ltd.
Inseego recalls USB8 4G Dongle Kit with outdated software that could cause video laryngoscope issues, delaying diagnosis and treatment. Affected units include Tempus Pro Monitor accessories with specific part numbers.
Remote Diagnostic Technologies recalls Tempus Pro Patient Monitors with specific model numbers due to a software error causing error screens when attaching video laryngoscopes. Affected units may display errors during use.
Philips recalls Tempus Pro Patient Monitors with software versions prior to vx.40 due to freezing issues and inaccurate 12-lead ECG readings. Affected models include 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007.
Remote Diagnostic Technologies recalls Tempus LS-Manual Defibrillator Model 00-3020 due to incorrect labels during servicing. Labels have wrong product names and CAT numbers, potentially causing misidentification. Affected units have specific serial numbers.
Philips recalls Tempus LS Manual Defibrillators (part 00-3020) when used with older user manuals. Distortions may cause ineffective pacing or defibrillation. Affected units have serial numbers before 7022.002871 or manual versions prior to 41-3007EN-01.
Philips recalls Tempus Pro Patient Monitors with specific hardware/software versions that may display error messages when laryngoscopes are unplugged, potentially delaying treatment or causing hypoxia.
Philips recalls Tempus LS Manual Defibrillators with part number 00-3020 that may show "HW failure DPM" error, causing ineffective pacing. Affected units have serial numbers before 7022.001634.
Remote Diagnostic Technologies recalls Tempus Pro Patient Monitors with specific model numbers and UDI-DI codes due to regulatory compliance issues involving fluid ingress and basic safety risks in power supplies.
Remote Diagnostic Technologies recalls Tempus LS defibrillators with specific software and serial numbers due to not being approved for US distribution. Affected units may pose safety risks.
Remote Diagnostic Technologies recalls Tempus Pro patient monitors with specific part numbers that can cause error messages when unplugged after use with a laryngoscope device.
Recall of Tempus LS manual defibrillators with software version 1.3.4 due to potential delay in therapy when switching between pacer and manual modes. Affected units have specific serial numbers.
