Device brand name · Wheelchair mechanical

Solara 3g Ltd 20w 24 Com 9153653250: medical device reports filed with FDA

168 reports name it, 2014–2016. Manufacturer given most often on reports: Invacare Taylor Street. Product code IOR.

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.

168
device reports naming the brand: 0% of all MAUDE reports · about 15 a year; 0
reports, 12 months to August 2026: 0 in the 12 months before; 98.2%
classified as malfunction: 89.3% across the product code; 0%
classified as death, as reported: 0 reports · not verified by FDA

168 medical device reports received by FDA name the brand "Solara 3g Ltd 20w 24 Com 9153653250" (wheelchair mechanical); the manufacturer given most often on reports is Invacare Taylor Street; received from December 2014 to June 2016. 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 (98.2%) and injury (1.8%); across all wheelchair, mechanical reports (product code IOR) death is recorded in 0.2% and malfunction in 89.3%. Event type is the reporter's classification of the report, not a verified outcome.

The device problems coded most often are break (31.5%), bent (17.3%) and device operates differently than expected (11.3%). The patient problems coded most often are injury and ulcer. 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 Solara 3g Ltd 20w 24 Com 9153653250 was received in the five years to August 2026; the latest was received in June 2016.

By year received

Event type and report source

Event type, as classified on the report

Death0%0

Injury1.8%3

Malfunction98.2%165

Other0%0

Not given0%0

Who filed the report

Manufacturer report100%168

Voluntary report0%0

User facility report0%0

Distributor report0%0

Not given0%0

Grey bar: all 28,715 reports carrying product code IOR. 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
Breakthe device broke	53	31.5%	29.9%
Bent	29	17.3%	6.6%
Device operates differently than expectedthe device behaved unexpectedly	19	11.3%	4.7%
Mechanical problema mechanical problem	15	8.9%	3.9%
Component missing	11	6.5%	1.3%
Crackthe device cracked	8	4.8%	4.1%
Device slipped	6	3.6%	2.9%
Mechanics altered	4	2.4%	0.8%
Detachment of device component	3	1.8%	4.5%
Loose or intermittent connection	3	1.8%	1.4%
Naturally worn	3	1.8%	1.5%
Out-of-box failure	3	1.8%	1%
Defective component	2	1.2%	0.3%
Fracturea broken bone	2	1.2%	5.2%
Improper or incorrect procedure or method	2	1.2%	0.3%
Stretched	2	1.2%	0.3%
Torn material	2	1.2%	1.5%
Unstable	2	1.2%	2.1%
Fitting problem	1	0.6%	0.2%
Material deformation	1	0.6%	0.6%

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
Injurya physical injury	1	0.6%
Ulcer	1	0.6%

Patient problem codes are present mainly in reports filed since 2019 and are often blank.

In context

Measure	Solara 3g Ltd 20w 24 Com 9153653250	Product code IOR	All MAUDE reports
Reports	168	28,715	26,136,888
Share of that pool	—	0.6%	0%
Classified as death, per 1,000 reports	0	2	9
Classified as injury	1.8%	3.7%	36.2%
Classified as malfunction	98.2%	89.3%	62.3%
Filed by the manufacturer	100%	96%	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 IOR

Brand	Reports	Latest 12 months	Classified as death
Mechanical Manual Wheelchair	10,279	0	0%
Quickie 2 Wheelchair	3,756	0	0%
Medline	26,935	26,184	0.1%
Transport 20 In X 16 In 9153637574	1,973	0	0.1%
Quickie	1,619	1	0.2%
Solara 3g Demo 3 Low Shear Recline/20 In H Matrx Pb Back	608	0	0%
9xt Swingaway Frame Style 9153629153	368	0	0%
Tracer Transport Chair 19 X 16 9153647029	342	0	0%
Breezy Wheelchair	334	0	0%
Quickie Rx Wheelchair	320	0	0%
Quickie Revolution Wheelchair	311	0	0%
T4/Wd28/Hd/Adult/18/Bh16/At903/U2222c/U67 9153653569	293	0	0%
Trsx5/Wd08/Ad/28/34p/U240/1255/U2222/Ahdrm/9691b/Gvt93hc/G1360/Bh16 9153649403	285	0	0%
Trex2/Wd06/18/Bh16/U2222c/Adult/U67/1255 9153653553	198	0	0%
Non-Folding Device 9153645342	151	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 Solara 3g Ltd 20w 24 Com 9153653250 reports

How many FDA reports name Solara 3g Ltd 20w 24 Com 9153653250?

168 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 (98.2%) and injury (1.8%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.

What device problems are coded?

break (31.5%), bent (17.3%), device operates differently than expected (11.3%), mechanical problem (8.9%) and component missing (6.5%). 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 Solara 3g Ltd 20w 24 Com 9153653250 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.