Devices › Set, administration, for peritoneal dialysis, disposable
Device brand name · Transfer set
Capd Solution Transfer Set Short For Uv-Flash: medical device reports filed with FDA
902 reports name it, 1997–2008. Manufacturer given most often on reports: Baxter Healthcare. Product code KDJ.
- 902
- device reports naming the brand
- 0% of all MAUDE reports · about 31 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 97.7%
- classified as malfunction
- 33% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
902 medical device reports received by FDA name the brand "Capd Solution Transfer Set Short For Uv-Flash" (transfer set); the manufacturer given most often on reports is Baxter Healthcare; received from March 1997 to November 2008. 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 (97.7%), injury (2.2%) and other (0.1%); across all set, administration, for peritoneal dialysis, disposable reports (product code KDJ) death is recorded in 3.3% and malfunction in 33%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are component(s), broken (25.9%), leak/splash (25.4%) and material separation (5.3%). The patient problems coded most often are treatment with medication(s), peritonitis and hospitalization required. 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 Capd Solution Transfer Set Short For Uv-Flash was received in the five years to August 2026; the latest was received in November 2008.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 72,328 reports carrying product code KDJ. 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 |
|---|---|---|---|
| Component(s), broken | 234 | 25.9% | 1.1% |
| Leak/splashthe device leaked | 229 | 25.4% | 3% |
| Material separation | 48 | 5.3% | 0.7% |
| Crackthe device cracked | 41 | 4.5% | 2.9% |
| Fluid/blood leak | 35 | 3.9% | 7.5% |
| Breakthe device broke | 34 | 3.8% | 2.1% |
| Detachment of device component | 22 | 2.4% | 0.8% |
| Hole in material | 17 | 1.9% | 0.3% |
| Replace | 15 | 1.7% | 1.2% |
| Tears, rips, holes in device, device material | 10 | 1.1% | 0.1% |
| Inappropriate waveform | 9 | 1% | 0% |
| Other (for use when an appropriate device code cannot be identified) | 8 | 0.9% | 0.2% |
| Sticking | 5 | 0.6% | 0% |
| Loose | 4 | 0.4% | 0.2% |
| Loose or intermittent connection | 4 | 0.4% | 1.3% |
| Misconnection | 4 | 0.4% | 0.1% |
| Source, detachment from | 4 | 0.4% | 0% |
| Disconnection | 3 | 0.3% | 4.4% |
| Bent | 2 | 0.2% | 0.1% |
| Component missing | 2 | 0.2% | 0.3% |
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 |
|---|---|---|
| Treatment with medication(s) | 22 | 2.4% |
| Peritonitis | 12 | 1.3% |
| Hospitalization required | 11 | 1.2% |
| Bacterial infectiona bacterial infection | 4 | 0.4% |
| No patient involvement | 4 | 0.4% |
| Therapy/non-surgical treatment, additional | 4 | 0.4% |
| Therapy/non-surgical treatment, aborted/stopped | 3 | 0.3% |
| Painpain, site not specified | 2 | 0.2% |
| Abdominal painstomach or belly pain | 1 | 0.1% |
| Blood loss | 1 | 0.1% |
| Confusion/ disorientation | 1 | 0.1% |
| Fever | 1 | 0.1% |
| Improved patient condition | 1 | 0.1% |
| Leak(s), perivalvular | 1 | 0.1% |
| Nauseafeeling sick | 1 | 0.1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Capd Solution Transfer Set Short For Uv-Flash | Product code KDJ | All MAUDE reports |
|---|---|---|---|
| Reports | 902 | 72,328 | 26,136,888 |
| Share of that pool | — | 1.2% | 0% |
| Classified as death, per 1,000 reports | 0 | 33 | 9 |
| Classified as injury | 2.2% | 63.6% | 36.2% |
| Classified as malfunction | 97.7% | 33% | 62.3% |
| Filed by the manufacturer | 100% | 99.6% | 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 KDJ
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Ni | 32,939 | 1,587 | 1.8% |
| MiniCap Transfer Set | 10,161 | 168 | 1.1% |
| MiniCap | 13,806 | 409 | 1.1% |
| Minicap Pd Transfer Set Easy-Lock With Twist Clamp | 1,903 | 0 | 0.1% |
| Renal - Disposable | 1,472 | 0 | 1.4% |
| Uv Flash Transfer Sets | 1,049 | 0 | 0% |
| Extension Set | 1,623 | 66 | 1.3% |
| Flexicap | 829 | 0 | 1.9% |
| Capd Disconnect Y Set | 685 | 0 | 1.6% |
| Minicap Extend Life Pd Transfset W/Twist Clamp | 603 | 0 | 0.3% |
| Minicap Disconnect Cap | 571 | 0 | 0.2% |
| Safe Lock Apd Luer Lock Connector | 511 | 0 | 0% |
| Locking Titanium Adapter | 494 | 5 | 1% |
| Uv-Flash Solution Transfer Set Short - Japan | 374 | 0 | 0% |
| Minicap Prep Kits | 441 | 4 | 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 Capd Solution Transfer Set Short For Uv-Flash reports
How many FDA reports name Capd Solution Transfer Set Short For Uv-Flash?
902 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 (97.7%), injury (2.2%) and other (0.1%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
component(s), broken (25.9%), leak/splash (25.4%), material separation (5.3%), crack (4.5%) and fluid/blood leak (3.9%). 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 Capd Solution Transfer Set Short For Uv-Flash 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.