Remote Diagnostic Technologies Ltd. recalls
Every recall we track for Remote Diagnostic Technologies Ltd. — 12 in all, from 2020–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Remote Diagnostic Technologies Ltd. doubled in 2025 (4, up from 2 in 2024).
All FDA recall records for Remote Diagnostic Technologies Ltd. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 1 | 0 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 1 | 1 |
| 2022 | 0 | 0 | 0 | 1 | 1 |
| 2023 | 0 | 2 | 1 | 0 | 3 |
| 2024 | 0 | 1 | 1 | 0 | 2 |
| 2025 | 0 | 1 | 3 | 0 | 4 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Remote Diagnostic Technologies Ltd. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Remote Diagnostic Technologies Ltd. recalls
12 shown- Lower riskMedical device
Remote Diagnostic Technologies Ltd. recalls 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
Remote Diagnostic Technologies Ltd. - Remote Diagnostic Technologies Ltd.
Remote Diagnostic Technologies Ltd.Nov 26, 2025 - Lower riskMedical device
Remote Diagnostic Technologies Ltd. recalls Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an
Inseego recalls USB8 4G Dongle Kit with outdated software that could cause video laryngoscope issues, delaying diagnosis and treatment.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.
InseegoMay 30, 2025 - Lower riskMedical device
Remote Diagnostic Technologies Ltd. recalls Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset dock), 00-1007-R and 00-1007
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.
Remote Diagnostic TechnologiesApr 16, 2025 - Use cautionMedical device
Remote Diagnostic Technologies Ltd. recalls Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007
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.
PhilipsApr 15, 2025 - Lower riskMedical device
Remote Diagnostic Technologies Ltd. recalls Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can deliver a shock in manual
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.
Remote Diagnostic TechnologiesOct 28, 2024 - Use cautionMedical device
Remote Diagnostic Technologies Ltd. recalls Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operator Manual
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.
PhilipsMay 9, 2024 - Use cautionMedical device
Remote Diagnostic Technologies Ltd. recalls 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
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.
PhilipsAug 24, 2023 - Use cautionMedical device
Remote Diagnostic Technologies Ltd. recalls Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020
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.
PhilipsMay 8, 2023 - Lower riskMedical device
Remote Diagnostic Technologies Ltd. recalls Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and medically qualified
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 TechnologiesFeb 23, 2023 - UnratedMedical device
Remote Diagnostic Technologies Ltd. recalls Tempus LS, Type DGE1, CAT 00-3010, REF 3.940590, Software version 1.3.5, UDI: (01)07613365001693
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 TechnologiesJan 28, 2022 - UnratedMedical device
Remote Diagnostic Technologies Ltd. recalls Tempus Pro - Patient physiological monitor, arrhythmia detector and alarm. Part No. - 00-1004-R, 00-1007-R, 00-1024-R,
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.
Remote Diagnostic TechnologiesMay 25, 2021 - Use cautionMedical device
Remote Diagnostic Technologies Ltd. recalls Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product Usage: The device is intended
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.
Remote Diagnostic TechnologiesNov 17, 2020
Remote Diagnostic Technologies Ltd. recall questions
How many recalls has Remote Diagnostic Technologies Ltd. had?
12 recalls from Remote Diagnostic Technologies Ltd. are on record with U.S. safety agencies, from 2020–2025.
What is the most recent Remote Diagnostic Technologies Ltd. recall?
Remote Diagnostic Technologies Ltd. recalls 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, dated Nov 26, 2025. Every Remote Diagnostic Technologies Ltd. recall is listed on this page, newest first.
What should I do if I have a recalled Remote Diagnostic Technologies Ltd. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Remote Diagnostic Technologies Ltd. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.