Devices › Detector and alarm, arrhythmia
Device brand name · Patient monitor
Mp70 Intellivue Patient Monitor: medical device reports filed with FDA
682 reports name it, 2005–2020. Manufacturer given most often on reports: Philips Medical Systems. Product code DSI.
- 682
- device reports naming the brand
- 0% of all MAUDE reports · about 33 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 65.1%
- classified as malfunction
- 90.5% across the product code
- 15.4%
- classified as death, as reported
- 105 reports · not verified by FDA
682 medical device reports received by FDA name the brand "Mp70 Intellivue Patient Monitor" (patient monitor); the manufacturer given most often on reports is Philips Medical Systems; received from September 2005 to December 2020. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
0 reports arrived in the 12 months to August 2026, and none 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 (65.1%), injury (19.1%) and death (15.4%); across all detector and alarm, arrhythmia reports (product code DSI) death is recorded in 1.5% and malfunction in 90.5%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are device alarm system (45%), no audible alarm (10.1%) and device operates differently than expected (8.7%). The patient problems coded most often are death, low oxygen saturation and cardiac arrest. 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
No report naming Mp70 Intellivue Patient Monitor was received in the five years to August 2026; the latest was received in December 2020.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 33,398 reports carrying product code DSI. 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 |
|---|---|---|---|
| Device alarm system | 307 | 45% | 2.9% |
| No audible alarm | 69 | 10.1% | 11.1% |
| Device operates differently than expectedthe device behaved unexpectedly | 59 | 8.7% | 2.9% |
| Device displays incorrect message | 50 | 7.3% | 1.5% |
| Component falling | 46 | 6.7% | 0.2% |
| Insufficient device problem information | 20 | 2.9% | 0.5% |
| Defective alarm | 19 | 2.8% | 0.7% |
| Detachment of device component | 17 | 2.5% | 0.1% |
| No display/image | 14 | 2.1% | 1.2% |
| Improper or incorrect procedure or method | 12 | 1.8% | 0.1% |
| Disconnection | 11 | 1.6% | 0.1% |
| Breakthe device broke | 10 | 1.5% | 0.2% |
| Alarm not visible | 7 | 1% | 0.1% |
| Display or visual feedback problem | 7 | 1% | 0.3% |
| Self-activation or keying | 7 | 1% | 0.3% |
| Communication or transmission problemthe device could not communicate or transmit | 6 | 0.9% | 3.3% |
| No audible prompt/feedback | 6 | 0.9% | 4.5% |
| Application interface becomes non-functional or program exits abnormally | 5 | 0.7% | 0.2% |
| Defective component | 5 | 0.7% | 0.2% |
| Device fell | 4 | 0.6% | 0% |
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 |
|---|---|---|
| Deaththe patient died; cause not stated by this term | 100 | 14.7% |
| Low oxygen saturation | 34 | 5% |
| Cardiac arrestthe heart stopped | 15 | 2.2% |
| Injurya physical injury | 12 | 1.8% |
| Bradycardiaslow heart rate | 10 | 1.5% |
| No patient involvement | 10 | 1.5% |
| Hemorrhage/blood loss/bleeding | 6 | 0.9% |
| Cardiopulmonary arrest | 5 | 0.7% |
| Head injurya head injury | 5 | 0.7% |
| Complaint, ill-defined | 4 | 0.6% |
| Ventricular tachycardiaa fast rhythm from the lower heart chambers | 4 | 0.6% |
| Cyanosis | 3 | 0.4% |
| Low blood pressure/ hypotension | 3 | 0.4% |
| Blood loss | 2 | 0.3% |
| Falla fall | 2 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Mp70 Intellivue Patient Monitor | Product code DSI | All MAUDE reports |
|---|---|---|---|
| Reports | 682 | 33,398 | 26,136,888 |
| Share of that pool | — | 2% | 0% |
| Classified as death, per 1,000 reports | 154 | 15 | 9 |
| Classified as injury | 19.1% | 7.8% | 36.2% |
| Classified as malfunction | 65.1% | 90.5% | 62.3% |
| Filed by the manufacturer | 99.9% | 99.3% | 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 DSI
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Reveal LINQ | 19,184 | 264 | 0% |
| MX40 1.4 GHz Smart Hopping | 5,135 | 6 | 1.3% |
| Reveal Xt | 2,037 | 0 | 0.1% |
| Mx40 2 4 Ghz Smart Hopping | 785 | 0 | 1.5% |
| Reveal Dx | 730 | 0 | 0.4% |
| Acuity Central Monitoring | 710 | 0 | 0% |
| IntelliVue Multi Measurement Server X2 | 1,924 | 135 | 1.7% |
| Intellivue Mx40 802 11a/B/G | 329 | 0 | 3% |
| Spacelabs Ultraview Sl Command Module | 200 | 4 | 8.5% |
| IntelliVue MX800 patient monitor | 502 | 54 | 10.6% |
| Patient Connector | 207 | 83 | 0% |
| IntelliVue MX40 2.4GHz | 192 | 56 | 6.8% |
| Passport 2 Monitor | 469 | 0 | 0.2% |
| IntelliVue MP5 | 261 | 73 | 10.7% |
| Zio AT | 711 | 90 | 3.5% |
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 Mp70 Intellivue Patient Monitor reports
How many FDA reports name Mp70 Intellivue Patient Monitor?
682 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
malfunction (65.1%), injury (19.1%) and death (15.4%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
device alarm system (45%), no audible alarm (10.1%), device operates differently than expected (8.7%), device displays incorrect message (7.3%) and component falling (6.7%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.9%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Mp70 Intellivue Patient Monitor 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.