Device brand name · Wheelchair powered
Power Chair 20 Wide By 18 Deep For Pmi: medical device reports filed with FDA
3,202 reports name it, 2014–2016. Manufacturer given most often on reports: Invacare Taylor Street. Product code ITI.
- 3,202
- device reports naming the brand
- 0% of all MAUDE reports · about 261 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 99.4%
- classified as malfunction
- 87.6% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 3,202 reports that name the brand "Power Chair 20 Wide By 18 Deep For Pmi" (wheelchair powered), received between April 2014 and December 2016; the manufacturer given most often on reports is Invacare Taylor Street. Spellings of one product vary from report to report.
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 (99.4%) and injury (0.4%); across all wheelchair, powered reports (product code ITI) death is recorded in 0.6% and malfunction in 87.6%. 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 (20.3%), break (13.5%) and mechanical problem (10.2%). The patient problems coded most often are fall, injury and bruise/contusion. 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 Power Chair 20 Wide By 18 Deep For Pmi was received in the five years to August 2026; the latest was received in December 2016.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 30,586 reports carrying product code ITI. 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 | 650 | 20.3% | 17.6% |
| Breakthe device broke | 432 | 13.5% | 12.5% |
| Mechanical problema mechanical problem | 328 | 10.2% | 6.6% |
| Bent | 168 | 5.2% | 3.4% |
| Device stops intermittentlythe device stopped now and then | 153 | 4.8% | 2.8% |
| Device slipped | 141 | 4.4% | 3.2% |
| Loss of powerthe device lost power | 141 | 4.4% | 3% |
| Device inoperablethe device could not be used | 133 | 4.2% | 3.6% |
| Failure to shut off | 133 | 4.2% | 4.6% |
| Device displays incorrect message | 126 | 3.9% | 3% |
| Unintended movement | 107 | 3.3% | 2.8% |
| Leak/splashthe device leaked | 100 | 3.1% | 5.1% |
| Detachment of device component | 92 | 2.9% | 3.1% |
| Noise, audible | 90 | 2.8% | 1.7% |
| Sticking | 88 | 2.7% | 3.4% |
| Crackthe device cracked | 83 | 2.6% | 1.6% |
| Mechanics altered | 67 | 2.1% | 1% |
| Self-activation or keying | 67 | 2.1% | 2.2% |
| Naturally worn | 64 | 2% | 1.3% |
| Loose or intermittent connection | 61 | 1.9% | 0.9% |
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 |
|---|---|---|
| Falla fall | 28 | 0.9% |
| Injurya physical injury | 14 | 0.4% |
| Bruise/contusion | 7 | 0.2% |
| Complaint, ill-defined | 6 | 0.2% |
| Laceration(s) | 5 | 0.2% |
| Painpain, site not specified | 5 | 0.2% |
| Bone fracture(s) | 4 | 0.1% |
| No patient involvement | 3 | 0.1% |
| Swellingswelling | 3 | 0.1% |
| Contusiona bruise | 2 | 0.1% |
| Physical entrapment | 2 | 0.1% |
| Pressure sore/ulcer | 2 | 0.1% |
| Tissue damage | 2 | 0.1% |
| Abrasion | 1 | 0% |
| Concussionconcussion | 1 | 0% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Power Chair 20 Wide By 18 Deep For Pmi | Product code ITI | All MAUDE reports |
|---|---|---|---|
| Reports | 3,202 | 30,586 | 26,136,888 |
| Share of that pool | — | 10.5% | 0% |
| Classified as death, per 1,000 reports | 0 | 6 | 9 |
| Classified as injury | 0.4% | 9.8% | 36.2% |
| Classified as malfunction | 99.4% | 87.6% | 62.3% |
| Filed by the manufacturer | 99.9% | 98.7% | 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 ITI
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Powered Wheelchair | 18,464 | 0 | 0.1% |
| Tdxsp Electric Red Euro Wide Base W/ 23-1 Ssd Gear Box | 1,309 | 0 | 0.2% |
| Pride Mobility Products | 1,939 | 145 | 3.6% |
| SmartDrive | 932 | 662 | 0% |
| M51p Blue Base W/Mk5 Nx Spj+ 9153642087 | 395 | 0 | 0% |
| Quickie | 1,619 | 1 | 0.2% |
| Tdxsp Wet Black Euro Narrow Base W/ 23-1 Ssd Gear Box | 270 | 0 | 0% |
| Invacare Power Wheelchair | 248 | 0 | 5.2% |
| Pride | 464 | 0 | 10.1% |
| Hoveround Corporation | 296 | 0 | 8.1% |
| Pronto M41 Blue Base 9153645762 | 185 | 0 | 0% |
| M51p Red Base W/Mk5 Nx Spj+ 9153642088 | 181 | 0 | 0% |
| Tdxsp Wet Black Euro Narrow Base W/ 18-1 Ssd Gear Box | 176 | 0 | 0% |
| Hoveround | 154 | 1 | 5.8% |
| Pronto M61 | 152 | 0 | 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 Power Chair 20 Wide By 18 Deep For Pmi reports
How many FDA reports name Power Chair 20 Wide By 18 Deep For Pmi?
3,202 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 (99.4%) and injury (0.4%). "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 (20.3%), break (13.5%), mechanical problem (10.2%), bent (5.2%) and device stops intermittently (4.8%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.9%) and distributor 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 Power Chair 20 Wide By 18 Deep For Pmi 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.