Devices › Pump, infusion, implanted, programmable
Device brand name · Lkk
Indura Catheter: medical device reports filed with FDA
373 reports name it, 2006–2016. Manufacturer given most often on reports: Rice Creek Manufacturing. Product code LKK.
- 373
- device reports naming the brand
- 0% of all MAUDE reports · about 19 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 40.5%
- classified as malfunction
- 32.6% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 373 reports that name the brand "Indura Catheter" (lkk), received between September 2006 and February 2016; the manufacturer given most often on reports is Rice Creek Manufacturing. Spellings of one product vary from report to report.
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 injury (59.2%), malfunction (40.5%) and other (0.3%); across all pump, infusion, implanted, programmable reports (product code LKK) death is recorded in 1.4% and malfunction in 32.6%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are replace (34.6%), explanted (26.3%) and device remains implanted (21.7%). The patient problems coded most often are surgical procedure, therapeutic response, decreased 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 Indura Catheter was received in the five years to August 2026; the latest was received in February 2016.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 117,271 reports carrying product code LKK. 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 |
|---|---|---|---|
| Replace | 129 | 34.6% | 3.5% |
| Explanted | 98 | 26.3% | 5.6% |
| Device remains implanted | 81 | 21.7% | 2.5% |
| Tears, rips, holes in device, device material | 62 | 16.6% | 0.5% |
| Fibrosis | 36 | 9.7% | 0.2% |
| Disconnection | 34 | 9.1% | 1.4% |
| Kinkedthe tube or line kinked | 33 | 8.8% | 1.5% |
| Occlusion within devicethe device blocked | 27 | 7.2% | 1.8% |
| Internal fixation, revision of | 23 | 6.2% | 0.1% |
| Dislodged | 22 | 5.9% | 0.4% |
| Device, or device fragments remain in patient | 15 | 4% | 0.3% |
| Repair | 15 | 4% | 0.4% |
| Fracturea broken bone | 14 | 3.8% | 0.5% |
| Migration or expulsion of device | 12 | 3.2% | 5.7% |
| Implant, removal of | 11 | 2.9% | 0.1% |
| Leak/splashthe device leaked | 11 | 2.9% | 0.5% |
| Improper or incorrect procedure or method | 7 | 1.9% | 4% |
| Breakthe device broke | 6 | 1.6% | 0.5% |
| Component(s), broken | 6 | 1.6% | 0.1% |
| Fluid/blood leak | 6 | 1.6% | 2.1% |
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 |
|---|---|---|
| Surgical procedure | 194 | 52% |
| Therapeutic response, decreased | 126 | 33.8% |
| Hospitalization required | 72 | 19.3% |
| Surgical procedure, additional | 44 | 11.8% |
| Inadequate pain relief | 42 | 11.3% |
| Painpain, site not specified | 34 | 9.1% |
| Granuloma | 33 | 8.8% |
| Treatment with medication(s) | 30 | 8% |
| Surgical procedure, repeated | 28 | 7.5% |
| Muscle spasm(s) | 20 | 5.4% |
| Therapy/non-surgical treatment, additional | 18 | 4.8% |
| Fibrosis | 17 | 4.6% |
| Identified diagnosis | 17 | 4.6% |
| Improved patient condition | 16 | 4.3% |
| Underdoseless than the intended dose | 13 | 3.5% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Indura Catheter | Product code LKK | All MAUDE reports |
|---|---|---|---|
| Reports | 373 | 117,271 | 26,136,888 |
| Share of that pool | — | 0.3% | 0% |
| Classified as death, per 1,000 reports | 0 | 14 | 9 |
| Classified as injury | 59.2% | 64% | 36.2% |
| Classified as malfunction | 40.5% | 32.6% | 62.3% |
| Filed by the manufacturer | 100% | 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."
Other brands with product code LKK
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Synchromed El | 7,189 | 2 | 4.9% |
| Synchromed | 3,429 | 3 | 3.2% |
| Indura | 2,730 | 0 | 0.8% |
| Intrathecal Catheter | 696 | 18 | 0.1% |
| Implantable Drug Infusion Pump | 649 | 177 | 0.9% |
| Ascenda | 570 | 14 | 0.9% |
| Infusion Pump | 830 | 6 | 3.7% |
| Prometra Programmable Pump | 348 | 0 | 6.6% |
| Intera 3000 | 307 | 99 | 0% |
| Isomed | 281 | 1 | 2.5% |
| Unknown Implantable Pump | 233 | 0 | 2.6% |
| N'vision | 269 | 0 | 0.7% |
| Implantable Infusion Pump | 211 | 0 | 3.8% |
| Unknown Infusion Pump | 157 | 0 | 1.9% |
| Catheter | 244 | 9 | 3.7% |
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 Indura Catheter reports
How many FDA reports name Indura Catheter?
373 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?
injury (59.2%), malfunction (40.5%) and other (0.3%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
replace (34.6%), explanted (26.3%), device remains implanted (21.7%), tears, rips, holes in device, device material (16.6%) and fibrosis (9.7%). 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 Indura Catheter 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.