Devices › Urinometer, electrical
Device brand name · Sensica device
Sensica Uo System: medical device reports filed with FDA
193 reports name it, 2021–2025. Manufacturer given most often on reports: C R Bard Covington -1018233. Product code EXS.
- 193
- device reports naming the brand
- 0% of all MAUDE reports · about 41 a year
- 1
- reports, 12 months to August 2026
- 8 in the 12 months before
- 98.4%
- classified as malfunction
- 99.4% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
193 medical device reports received by FDA name the brand "Sensica Uo System" (sensica device); the manufacturer given most often on reports is C R Bard Covington -1018233; received from October 2021 to September 2025. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
1 reports arrived in the 12 months to August 2026, down 87% from 8 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 (98.4%) and injury (1.6%); across all urinometer, electrical reports (product code EXS) death is recorded in 0% and malfunction in 99.4%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are device sensing problem (28.5%), volume accuracy problem (16.6%) and component misassembled (13%). The patient problems coded most often are appropriate clinical signs, symptoms and conditions term/code not available. 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
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 464 reports carrying product code EXS. 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 sensing problem | 55 | 28.5% | 19.8% |
| Volume accuracy problem | 32 | 16.6% | 22.2% |
| Component misassembled | 25 | 13% | 7.3% |
| Computer software problema software problem | 16 | 8.3% | 6.9% |
| Display or visual feedback problem | 14 | 7.3% | 10.8% |
| Restricted flow rate | 11 | 5.7% | 4.3% |
| Failure to calibrate | 7 | 3.6% | 2.2% |
| Operating system becomes nonfunctional | 7 | 3.6% | 5.2% |
| Erratic or intermittent display | 5 | 2.6% | 3% |
| Breakthe device broke | 4 | 2.1% | 2.6% |
| Defective component | 4 | 2.1% | 1.9% |
| Intermittent loss of power | 4 | 2.1% | 1.5% |
| Computer operating system problem | 3 | 1.6% | 3.7% |
| Failure to power up | 3 | 1.6% | 1.3% |
| Circuit failure | 2 | 1% | 2.4% |
| Device handling problem | 2 | 1% | 1.5% |
| Failure to sense | 2 | 1% | 0.9% |
| Fitting problem | 2 | 1% | 0.6% |
| Incorrect, inadequate or imprecise result or readings | 2 | 1% | 4.5% |
| Material fragmentation | 2 | 1% | 1.7% |
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 |
|---|---|---|
| Appropriate clinical signs, symptoms and conditions term/code not available | 41 | 21.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Sensica Uo System | Product code EXS | All MAUDE reports |
|---|---|---|---|
| Reports | 193 | 464 | 26,136,888 |
| Share of that pool | — | 41.6% | 0% |
| Classified as death, per 1,000 reports | 0 | 0 | 9 |
| Classified as injury | 1.6% | 0.6% | 36.2% |
| Classified as malfunction | 98.4% | 99.4% | 62.3% |
| Filed by the manufacturer | 97.9% | 99.1% | 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."
Questions about Sensica Uo System reports
How many FDA reports name Sensica Uo System?
193 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 1 in the latest 12 months.
What kinds of events are reported?
malfunction (98.4%) and injury (1.6%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
device sensing problem (28.5%), volume accuracy problem (16.6%), component misassembled (13%), computer software problem (8.3%) and display or visual feedback problem (7.3%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (97.9%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Sensica Uo System 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.