Device brand name
Daily Activity Assist Devices: medical device reports filed with FDA
3,385 reports name it, 2011–2014. Manufacturer given most often on reports: Invamex. Product code IKX.
- 3,385
- device reports naming the brand
- 0% of all MAUDE reports · about 224 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 36.9%
- classified as malfunction
- 29.2% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
3,385 medical device reports received by FDA name the brand "Daily Activity Assist Devices"; the manufacturer given most often on reports is Invamex; received from June 2011 to November 2014. 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 (36.9%) and injury (0.4%); across all aid, transfer reports (product code IKX) death is recorded in 1% and malfunction in 29.2%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are crack (36.5%), break (24.9%) and unstable (11.2%). 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 Daily Activity Assist Devices was received in the five years to August 2026; the latest was received in November 2014.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 2,540 reports carrying product code IKX. 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 |
|---|---|---|---|
| Crackthe device cracked | 1,236 | 36.5% | 24.2% |
| Breakthe device broke | 844 | 24.9% | 27.9% |
| Unstable | 380 | 11.2% | 11.3% |
| Bent | 337 | 10% | 9.6% |
| Product quality problem | 192 | 5.7% | 5.4% |
| Detachment of device component | 110 | 3.2% | 3.8% |
| Collapse | 96 | 2.8% | 3.4% |
| Deformation due to compressive stress | 78 | 2.3% | 3% |
| Device operates differently than expectedthe device behaved unexpectedly | 65 | 1.9% | 2.1% |
| Out-of-box failure | 25 | 0.7% | 0.3% |
| Unintended movement | 23 | 0.7% | 0.7% |
| Device slipped | 20 | 0.6% | 3% |
| Split | 19 | 0.6% | 0.4% |
| Torn material | 19 | 0.6% | 0.6% |
| Component falling | 16 | 0.5% | 0.2% |
| Component missing | 14 | 0.4% | 0.4% |
| Naturally worn | 14 | 0.4% | 0.5% |
| Hole in material | 10 | 0.3% | 0.2% |
| Mechanical problema mechanical problem | 9 | 0.3% | 0.6% |
| Insufficient device problem information | 8 | 0.2% | 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 |
|---|---|---|
| Falla fall | 211 | 6.2% |
| Injurya physical injury | 79 | 2.3% |
| Bruise/contusion | 49 | 1.4% |
| Discomfortdiscomfort | 33 | 1% |
| Laceration(s) | 18 | 0.5% |
| Skin tears | 14 | 0.4% |
| Abrasion | 11 | 0.3% |
| Complaint, ill-defined | 11 | 0.3% |
| No patient involvement | 11 | 0.3% |
| Head injurya head injury | 4 | 0.1% |
| Bone fracture(s) | 3 | 0.1% |
| Erythemaskin redness | 3 | 0.1% |
| Heartburn/indigestion | 3 | 0.1% |
| Hemorrhage/blood loss/bleeding | 3 | 0.1% |
| Painpain, site not specified | 3 | 0.1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Daily Activity Assist Devices | Product code IKX | All MAUDE reports |
|---|---|---|---|
| Reports | 3,385 | 2,540 | 26,136,888 |
| Share of that pool | — | 133.3% | 0% |
| Classified as death, per 1,000 reports | 0 | 10 | 9 |
| Classified as injury | 0.4% | 2.6% | 36.2% |
| Classified as malfunction | 36.9% | 29.2% | 62.3% |
| Filed by the manufacturer | 100% | 95.4% | 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 IKX
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Guardian | 557 | 350 | 0.4% |
| Apex | 876 | 78 | 1.3% |
| Mechanical Walker Rollator | 5,681 | 0 | 0% |
| Rollator 9153651315 | 826 | 0 | 0% |
| Surgistool | 389 | 11 | 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 Daily Activity Assist Devices reports
How many FDA reports name Daily Activity Assist Devices?
3,385 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 (36.9%) and injury (0.4%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
crack (36.5%), break (24.9%), unstable (11.2%), bent (10%) and product quality problem (5.7%). 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 Daily Activity Assist Devices 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.