Devices › Ventilator, continuous, facility use
Device brand name · Ventilators intensive care
Evita V800: medical device reports filed with FDA
159 reports name it, 2020–2026. Product code CBK.
- 159
- device reports naming the brand
- 0% of all MAUDE reports · about 27 a year
- 48
- reports, 12 months to August 2026
- 25 in the 12 months before
- 90.6%
- classified as malfunction
- 91.8% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 159 reports that name the brand "Evita V800" (ventilators intensive care), received between August 2020 and August 2026. Spellings of one product vary from report to report.
48 reports arrived in the 12 months to August 2026, up 92% from 25 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 (90.6%) and injury (9.4%); across all ventilator, continuous, facility use reports (product code CBK) death is recorded in 1.1% and malfunction in 91.8%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are failure to deliver (37.1%), gas output problem (34.6%) and decrease in pressure (30.8%). The patient problems coded most often are low oxygen saturation, cardiac arrest and increased respiratory rate. 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 213,387 reports carrying product code CBK. 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 |
|---|---|---|---|
| Failure to deliverthe device did not deliver the dose or item | 59 | 37.1% | 1.2% |
| Gas output problem | 55 | 34.6% | 0.7% |
| Decrease in pressure | 49 | 30.8% | 0.8% |
| Device difficult to program or calibrate | 36 | 22.6% | 0.1% |
| No display/image | 35 | 22% | 5.2% |
| Reset problem | 23 | 14.5% | 0.2% |
| Display or visual feedback problem | 14 | 8.8% | 1.6% |
| Complete loss of power | 12 | 7.5% | 0.4% |
| Unexpected shutdown | 11 | 6.9% | 1.1% |
| Intermittent communication failure | 10 | 6.3% | 0.1% |
| Human-device interface problem | 8 | 5% | 0.1% |
| Output problem | 7 | 4.4% | 6% |
| Failure to sense | 6 | 3.8% | 0.1% |
| Imprecise or erratic results | 5 | 3.1% | 0% |
| Insufficient device problem information | 4 | 2.5% | 1.2% |
| Complete blockage | 3 | 1.9% | 0% |
| Data problem | 3 | 1.9% | 0% |
| Image display error/artifact | 3 | 1.9% | 0.3% |
| Inaccurate delivery | 3 | 1.9% | 0.4% |
| Device alarm system | 2 | 1.3% | 1.8% |
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 |
|---|---|---|
| Low oxygen saturation | 8 | 5% |
| Cardiac arrestthe heart stopped | 4 | 2.5% |
| Increased respiratory rate | 2 | 1.3% |
| Respiratory arrestbreathing stopped | 2 | 1.3% |
| Apnea | 1 | 0.6% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 1 | 0.6% |
| Bradycardiaslow heart rate | 1 | 0.6% |
| Coughcough | 1 | 0.6% |
| Cyanosis | 1 | 0.6% |
| Headachehead pain | 1 | 0.6% |
| Hypoxialow oxygen | 1 | 0.6% |
| Therapeutic effects, unexpected | 1 | 0.6% |
| Ventilator dependent | 1 | 0.6% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Evita V800 | Product code CBK | All MAUDE reports |
|---|---|---|---|
| Reports | 159 | 213,387 | 26,136,888 |
| Share of that pool | — | 0.1% | 0% |
| Classified as death, per 1,000 reports | 0 | 11 | 9 |
| Classified as injury | 9.4% | 6.8% | 36.2% |
| Classified as malfunction | 90.6% | 91.8% | 62.3% |
| Filed by the manufacturer | 98.7% | 95.9% | 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 CBK
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Trilogy 100 | 31,022 | 2,056 | 0.9% |
| 840 Ventilator | 18,191 | 27 | 0.4% |
| Hamilton Medical Ag | 10,331 | 0 | 0.3% |
| Trilogy Evo | 8,583 | 943 | 1.1% |
| Vela Ventilator | 8,446 | 0 | 0.3% |
| Servo-I | 6,390 | 3 | 1.3% |
| Esprit Ventilator | 6,015 | 0 | 0.4% |
| Vocsn | 5,308 | 854 | 0.4% |
| Trilogy 202 | 5,217 | 74 | 0.3% |
| Carescape R860 | 4,968 | 50 | 0.2% |
| Carescape | 4,902 | 2,289 | 0.1% |
| 980 Ventilator | 4,651 | 117 | 0.2% |
| Trilogy O2 | 4,290 | 48 | 0.3% |
| Avea Ventilator | 3,943 | 0 | 0.5% |
| V200 Ventilator | 3,476 | 0 | 0.2% |
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 Evita V800 reports
How many FDA reports name Evita V800?
159 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 48 in the latest 12 months.
What kinds of events are reported?
malfunction (90.6%) and injury (9.4%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
failure to deliver (37.1%), gas output problem (34.6%), decrease in pressure (30.8%), device difficult to program or calibrate (22.6%) and no display/image (22%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (98.7%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Evita V800 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.