Devices › Monitor, physiological, patient(with arrhythmia detection or alarms)
Device brand name · Monitor physiological patient with arrhythmia detection or alarms
Tempus Pro: medical device reports filed with FDA
1,850 reports name it, 2022–2026. Manufacturer given most often on reports: Remote Diagnostic Technologies. Product code MHX.
- 1,850
- device reports naming the brand
- 0% of all MAUDE reports · about 473 a year
- 108
- reports, 12 months to August 2026
- 597 in the 12 months before
- 98.4%
- classified as malfunction
- 82.1% across the product code
- 0.5%
- classified as death, as reported
- 9 reports · not verified by FDA
FDA's MAUDE database holds 1,850 reports that name the brand "Tempus Pro" (monitor physiological patient with arrhythmia detection or alarms), received between August 2022 and August 2026; the manufacturer given most often on reports is Remote Diagnostic Technologies. Spellings of one product vary from report to report.
108 reports arrived in the 12 months to August 2026, down 82% from 597 in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (98.4%), injury (1.1%) and death (0.5%); across all monitor, physiological, patient(with arrhythmia detection or alarms) reports (product code MHX) death is recorded in 5.9% and malfunction in 82.1%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are unable to obtain readings (17.5%), display or visual feedback problem (9%) and failure to charge (8.9%). The patient problems coded most often are cardiac arrest, chest pain and hemodynamic instability. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 32,636 reports carrying product code MHX. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Unable to obtain readings | 324 | 17.5% | 2.3% |
| Display or visual feedback problem | 167 | 9% | 3.2% |
| Failure to charge | 165 | 8.9% | 0.8% |
| Erratic or intermittent display | 119 | 6.4% | 0.9% |
| Charging problem | 106 | 5.7% | 0.6% |
| Unexpected shutdown | 100 | 5.4% | 1.4% |
| Breakthe device broke | 89 | 4.8% | 1.4% |
| Failure to power up | 83 | 4.5% | 0.7% |
| Operating system becomes nonfunctional | 68 | 3.7% | 0.6% |
| Loose or intermittent connection | 49 | 2.6% | 0.3% |
| Material integrity problema problem with the device material | 48 | 2.6% | 0.3% |
| No display/image | 47 | 2.5% | 4.1% |
| Failure to calibrate | 46 | 2.5% | 0.3% |
| Mechanical problema mechanical problem | 43 | 2.3% | 0.5% |
| Computer software problema software problem | 39 | 2.1% | 0.8% |
| Incorrect, inadequate or imprecise result or readings | 38 | 2.1% | 1.2% |
| Electrical /electronic property probleman electrical or electronic problem | 35 | 1.9% | 0.6% |
| Incorrect measurementthe device measured wrongly | 35 | 1.9% | 1.7% |
| Fracturea broken bone | 29 | 1.6% | 0.2% |
| Insufficient device problem information | 28 | 1.5% | 1.3% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Cardiac arrestthe heart stopped | 38 | 2.1% |
| Chest painchest pain | 4 | 0.2% |
| Hemodynamic instability | 2 | 0.1% |
| Myocardial infarctionheart attack | 2 | 0.1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Tempus Pro | Product code MHX | All MAUDE reports |
|---|---|---|---|
| Reports | 1,850 | 32,636 | 26,136,888 |
| Share of that pool | — | 5.7% | 0% |
| Classified as death, per 1,000 reports | 5 | 59 | 9 |
| Classified as injury | 1.1% | 11.2% | 36.2% |
| Classified as malfunction | 98.4% | 82.1% | 62.3% |
| Filed by the manufacturer | 99.9% | 93.4% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code MHX
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Patient Information Center iX | 1,941 | 619 | 10.4% |
| uCor Heart Failure and Arrhythmia Management System | 1,877 | 762 | 0% |
| Cns-6201a | 1,720 | 0 | 0.8% |
| IntelliVue Multi Measurement Server X2 | 1,924 | 135 | 1.7% |
| Cns-6801a | 1,058 | 0 | 1.5% |
| Intellivue Information Center Ix | 952 | 0 | 7.5% |
| Intellivue X3 | 777 | 0 | 1.5% |
| Tempus Pro, Printer | 562 | 400 | 0% |
| Piic Ix Hardware | 538 | 0 | 4.6% |
| Xhibit Central Station | 492 | 154 | 0.8% |
| IntelliVue Multi-Measurement Module X3 | 478 | 401 | 1.7% |
| IntelliVue MX450 Patient Monitor | 448 | 123 | 7.6% |
| Pu-681ra | 437 | 222 | 1.4% |
| Cns-9700a | 393 | 0 | 0.3% |
| Arrhythmia Management System | 381 | 4 | 0% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Tempus Pro reports
How many FDA reports name Tempus Pro?
1,850 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 108 in the latest 12 months.
What kinds of events are reported?
malfunction (98.4%), injury (1.1%) and death (0.5%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
unable to obtain readings (17.5%), display or visual feedback problem (9%), failure to charge (8.9%), erratic or intermittent display (6.4%) and charging problem (5.7%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.9%) and voluntary reports (0.1%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Tempus Pro was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.