Devices › Monitor, physiological, patient(with arrhythmia detection or alarms)
Device brand name · Monitor physiological patient with arrhythmia detection or alarms
Tempus Pro, Printer, IBP: medical device reports filed with FDA
230 reports name it, 2025–2026. Manufacturer given most often on reports: Remote Diagnostic Technologies. Product code MHX.
- 230
- device reports naming the brand
- 0% of all MAUDE reports · about 173 a year
- 187
- reports, 12 months to August 2026
- 43 in the 12 months before
- 100%
- classified as malfunction
- 82.1% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
230 medical device reports received by FDA name the brand "Tempus Pro, Printer, IBP" (monitor physiological patient with arrhythmia detection or alarms); the manufacturer given most often on reports is Remote Diagnostic Technologies; received from March 2025 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
187 reports arrived in the 12 months to August 2026, up 335% from 43 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 (100%); 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 break (17.8%), unable to obtain readings (11.3%) and failure to charge (10.9%). The patient problems coded most often are bradycardia, cardiac arrest and hypoxia. 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.
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 |
|---|---|---|---|
| Breakthe device broke | 41 | 17.8% | 1.4% |
| Unable to obtain readings | 26 | 11.3% | 2.3% |
| Failure to charge | 25 | 10.9% | 0.8% |
| Erratic or intermittent display | 22 | 9.6% | 0.9% |
| Charging problem | 21 | 9.1% | 0.6% |
| Display or visual feedback problem | 17 | 7.4% | 3.2% |
| Operating system becomes nonfunctional | 16 | 7% | 0.6% |
| Fracturea broken bone | 12 | 5.2% | 0.2% |
| Crackthe device cracked | 10 | 4.3% | 0.1% |
| Mechanical problema mechanical problem | 7 | 3% | 0.5% |
| Material integrity problema problem with the device material | 6 | 2.6% | 0.3% |
| Communication or transmission problemthe device could not communicate or transmit | 5 | 2.2% | 6% |
| Computer operating system problem | 5 | 2.2% | 1.9% |
| Computer software problema software problem | 5 | 2.2% | 0.8% |
| Wireless communication problema wireless connection problem | 5 | 2.2% | 1.5% |
| Incorrect measurementthe device measured wrongly | 4 | 1.7% | 1.7% |
| No tactile prompts/feedback | 4 | 1.7% | 0.1% |
| Imprecise or erratic results | 3 | 1.3% | 0.4% |
| Poor quality image | 3 | 1.3% | 0.1% |
| Power problem | 3 | 1.3% | 1.6% |
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 |
|---|---|---|
| Bradycardiaslow heart rate | 1 | 0.4% |
| Cardiac arrestthe heart stopped | 1 | 0.4% |
| Hypoxialow oxygen | 1 | 0.4% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Tempus Pro, Printer, IBP | Product code MHX | All MAUDE reports |
|---|---|---|---|
| Reports | 230 | 32,636 | 26,136,888 |
| Share of that pool | — | 0.7% | 0% |
| Classified as death, per 1,000 reports | 0 | 59 | 9 |
| Classified as injury | 0% | 11.2% | 36.2% |
| Classified as malfunction | 100% | 82.1% | 62.3% |
| Filed by the manufacturer | 100% | 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% |
| Tempus Pro | 1,850 | 108 | 0.5% |
| 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% |
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, Printer, IBP reports
How many FDA reports name Tempus Pro, Printer, IBP?
230 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 187 in the latest 12 months.
What kinds of events are reported?
malfunction (100%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
break (17.8%), unable to obtain readings (11.3%), failure to charge (10.9%), erratic or intermittent display (9.6%) and charging problem (9.1%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Tempus Pro, Printer, IBP 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.