Vehicle, motorized 3-wheeled: medical device reports filed with FDA

2,720 reports carry this product code, 1993–2026; 11 brands with a page.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "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."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

2,720
reports with this product code: 0% of all MAUDE reports; 31
reports, 12 months to August 2026: 28 in the 12 months before; 22.9%
classified as malfunction: 62.3% across all reports; 2.7%
classified as death, as reported: 0.9% across all reports

Product code INI is FDA's classification for "Vehicle, motorized 3-wheeled" (physical Medicine panel), a class 2 device. 2,720 medical device reports carry this product code, 0% of the MAUDE database, from May 1993 to August 2026.

31 reports arrived in the 12 months to August 2026, up 11% from 28 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 injury (33.3%), malfunction (22.9%) and other (5.9%). 11 brand names with a page on this site carry this code; the brands table is 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."

Brands with this product code

Brand	Reports	Latest 12 months	Classified as death	Classified as malfunction
Motorized 3-Wheeled Vehicle For Outside Transport	1,036	0	0.1%	12.5%
Pride Mobility Products	455	145	3.6%	17.4%
Rascal	411	0	2.2%	33.7%
Pride	168	0	10.1%	2.6%
Hoveround Corporation	62	0	8.1%	0%
Drive	19	20	4.4%	13.1%
Drive Medical	9	0	10%	5.2%
Mechanical Chair/Transport Chair	6	0	0.2%	11%
Sterling	4	300	0.1%	95.6%
Hoveround	1	1	5.8%	0%
Sftwr Css7201 Guardian Android App	1	2	0%	100%

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."

Manufacturers named

Manufacturer (as written on reports)	Reports	Share
Pride Mobility Products	612	22.5%
Invacare Taylor Street	80	2.9%
Invacare	15	0.6%
Danyang Maxthai Medical Equipment	6	0.2%
Invacare Rehabilitation Equip	1	0%
Stryker Medical Div	1	0%

Reports by month, five years

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

Death2.7%74

Injury33.3%906

Malfunction22.9%623

Other5.9%161

Not given35.1%956

Who filed

Manufacturer report89.6%2,436

Voluntary report4.6%126

User facility report0%0

Distributor report5.4%147

Not given0.4%11

Grey bar: all 26,136,888 MAUDE reports.

Device problems coded

Device problem (FDA code)	Reports	Share
Device tipped over	217	8%
Breakthe device broke	206	7.6%
Product quality problem	173	6.4%
Device operates differently than expectedthe device behaved unexpectedly	164	6%
Device stops intermittentlythe device stopped now and then	158	5.8%
Unintended movement	133	4.9%
Unstable	117	4.3%
Other (for use when an appropriate device code cannot be identified)	98	3.6%
Unintended system motionthe device moved when it should not have	93	3.4%
Fire	89	3.3%
Device inoperablethe device could not be used	85	3.1%
Crackthe device cracked	70	2.6%
Component(s), broken	60	2.2%
Detachment of device component	59	2.2%
Fracturea broken bone	49	1.8%
Loss of powerthe device lost power	46	1.7%
Improper or incorrect procedure or method	43	1.6%
Insufficient device problem information	43	1.6%
Self-activation or keying	39	1.4%
Unintended collision	33	1.2%

Questions about vehicle, motorized 3-wheeled reports

What is product code INI?

FDA's classification code for "Vehicle, motorized 3-wheeled", class 2, reviewed by the physical Medicine panel. Every device report carries the product code of the device involved.

How many reports carry this code?

2,720 reports through August 2026, 31 of them in the latest 12 months.

Which brands appear most often?

Motorized 3-Wheeled Vehicle For Outside Transport (1,036), Pride Mobility Products (455), Rascal (411), Pride (168) and Hoveround Corporation (62). Widely used products collect more reports because more people use them.

Can the brands table be used to rank the devices?

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." Brands differ in how many are in use, how long they have been sold and how reports are collected.

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. 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.