Devices › Ventilator, continuous, facility use
Device brand name · Ventilator continuous facility use
V200 Ventilator: medical device reports filed with FDA
3,476 reports name it, 2010–2021. Manufacturer given most often on reports: Respironics California. Product code CBK.
- 3,476
- device reports naming the brand
- 0% of all MAUDE reports · about 211 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 99.1%
- classified as malfunction
- 91.8% across the product code
- 0.2%
- classified as death, as reported
- 6 reports · not verified by FDA
3,476 medical device reports received by FDA name the brand "V200 Ventilator" (ventilator continuous facility use); the manufacturer given most often on reports is Respironics California; received from January 2010 to March 2021. 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 (99.1%), injury (0.7%) and death (0.2%); 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 device operates differently than expected (13.4%), failure to power up (12.1%) and device displays incorrect message (11.2%). The patient problems coded most often are no patient involvement, death and low oxygen saturation. 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 V200 Ventilator was received in the five years to August 2026; the latest was received in March 2021.
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 |
|---|---|---|---|
| Device operates differently than expectedthe device behaved unexpectedly | 465 | 13.4% | 5.5% |
| Failure to power up | 422 | 12.1% | 2.9% |
| Device displays incorrect message | 390 | 11.2% | 9% |
| Device inoperablethe device could not be used | 331 | 9.5% | 4.3% |
| No display/image | 180 | 5.2% | 5.2% |
| Battery problema problem with the battery | 158 | 4.5% | 4.5% |
| Loss of powerthe device lost power | 152 | 4.4% | 1.5% |
| Defective component | 127 | 3.7% | 2.1% |
| Incorrect, inadequate or imprecise result or readings | 112 | 3.2% | 0.3% |
| Defective devicethe device was defective | 96 | 2.8% | 0.2% |
| Device alarm system | 95 | 2.7% | 1.8% |
| Therapeutic or diagnostic output failure | 95 | 2.7% | 0.4% |
| Computer operating system problem | 92 | 2.6% | 0.2% |
| Power problem | 89 | 2.6% | 1.4% |
| Failure of device to self-test | 85 | 2.4% | 2.2% |
| Display or visual feedback problem | 72 | 2.1% | 1.6% |
| Tidal volume fluctuations | 67 | 1.9% | 0.5% |
| Breakthe device broke | 56 | 1.6% | 0.6% |
| Failure to charge | 52 | 1.5% | 2.5% |
| Output problem | 43 | 1.2% | 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 |
|---|---|---|
| No patient involvement | 2,020 | 58.1% |
| Deaththe patient died; cause not stated by this term | 7 | 0.2% |
| Low oxygen saturation | 4 | 0.1% |
| Bradycardiaslow heart rate | 1 | 0% |
| Burn, thermal | 1 | 0% |
| Cardiac arrestthe heart stopped | 1 | 0% |
| Cyanosis | 1 | 0% |
| Diaphoresis | 1 | 0% |
| Dyspneashortness of breath | 1 | 0% |
| Electric shockan electric shock | 1 | 0% |
| Inadequate osseointegration | 1 | 0% |
| Injurya physical injury | 1 | 0% |
| Respiratory failurethe lungs could not supply enough oxygen | 1 | 0% |
| Suffocation | 1 | 0% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | V200 Ventilator | Product code CBK | All MAUDE reports |
|---|---|---|---|
| Reports | 3,476 | 213,387 | 26,136,888 |
| Share of that pool | — | 1.6% | 0% |
| Classified as death, per 1,000 reports | 2 | 11 | 9 |
| Classified as injury | 0.7% | 6.8% | 36.2% |
| Classified as malfunction | 99.1% | 91.8% | 62.3% |
| Filed by the manufacturer | 100% | 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% |
| Uni-Vent Model 731 | 3,305 | 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 V200 Ventilator reports
How many FDA reports name V200 Ventilator?
3,476 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 (99.1%), injury (0.7%) and death (0.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
device operates differently than expected (13.4%), failure to power up (12.1%), device displays incorrect message (11.2%), device inoperable (9.5%) and no display/image (5.2%). 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 V200 Ventilator 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.