Brand

Remote Diagnostic Technologies Ltd. Recalls

8 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Remote Diagnostic Technologies Ltd..

8Total Recalls
0Critical
26,731Units Affected
Nov 26, 2025Most Recent
All Recalls

Every Remote Diagnostic Technologies Ltd. Recall

Sorted by most recent. Click any recall for full details.

8 recalls
High RiskFDA
Remote Diagnostic Technologies Ltd.
Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel IBP Module, REF: ...
Medical Devices·7,129 affected·Nov 26, 2025
High RiskFDA
Remote Diagnostic Technologies Ltd.
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007
Medical Devices·6,961 affected·Apr 15, 2025
High RiskFDA
Remote Diagnostic Technologies Ltd.
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual
Cardiac Devices·1,745 affected·May 9, 2024
High RiskFDA
Remote Diagnostic Technologies Ltd.
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00-1007, when Used With Tempus Pro Vide...
Medical Devices·3,524 affected·Aug 24, 2023
High RiskFDA
Remote Diagnostic Technologies Ltd.
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
Cardiac Devices·1,147 affected·May 8, 2023
High RiskFDA
Remote Diagnostic Technologies Ltd.
Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified personnel, for the...
Medical Devices·5,540 affected·Feb 23, 2023
High RiskFDA
Remote Diagnostic Technologies Ltd.
Tempus Pro - Patient physiological monitor, arrhythmia detector and alarm. Part No. - 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. Produ...
Medical Devices·510 affected·May 25, 2021
High RiskFDA
Remote Diagnostic Technologies Ltd.
Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product Usage: The device is intended to be used in th...
Cardiac Devices·175 affected·Nov 17, 2020