Remote Diagnostic Technologies Ltd.
Complete recall history across all FDA and CPSC categories — 12 total recalls
Remote Diagnostic Technologies Ltd. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (12)
FDA medical device enforcement actions by Remote Diagnostic Technologies Ltd.
| Date | Product | Reason | Class |
|---|---|---|---|
| Nov 26, 2025 | Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007... | Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BD... | Class II |
| May 30, 2025 | Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Dr... | Kit USB flash drive contains outdated software, which could result in reverti... | Class II |
| Apr 16, 2025 | Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, wi... | software issue that causes an error screen on a portable vital signs monitor ... | Class II |
| Apr 15, 2025 | Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00... | Patient Monitor software update to address issues:1)May freeze at startup wit... | Class II |
| Oct 28, 2024 | Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a de... | Due to incorrect labels applied to devices during servicing. Labels contain ... | Class III |
| May 9, 2024 | Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempu... | Simultaneous ECG measurements with multiple devices, including a manual defib... | Class II |
| Aug 24, 2023 | Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-... | Full screen error message may occur on patient monitors with affected hardwar... | Class II |
| May 8, 2023 | Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 | Defibrillator/pacemaker module (DPM) may encounter a problem causing communic... | Class II |
| Feb 23, 2023 | Tempus Pro Patient Monitor is a portable vital signs monitor intended to be u... | During internal testing, Regulatory Compliance issues were identified regardi... | Class II |
| Jan 28, 2022 | Tempus LS, Type DGE1, CAT 00-3010, REF 3.940590, Software version 1.3.5, UDI:... | Distribution of Defibrillators that are not approved or cleared for distribu... | Class II |
| May 25, 2021 | Tempus Pro - Patient physiological monitor, arrhythmia detector and alarm. ... | The Tempus Pro (Trizeps 7 only) when used in combination with a specified lar... | Class II |
| Nov 17, 2020 | Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.... | A software error was detected within software version 1.3.4 for the Tempus LS... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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