Devices › Pump, infusion, implanted, programmable
Device brand name · Pump infusion implanted programmable
Implantable Infusion Pump: medical device reports filed with FDA
211 reports name it, 2015–2019. Manufacturer given most often on reports: Medtronic Neuromodulation. Product code LKK.
- 211
- 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
- 11.4%
- classified as malfunction
- 32.6% across the product code
- 3.8%
- classified as death, as reported
- 8 reports · not verified by FDA
FDA's MAUDE database holds 211 reports that name the brand "Implantable Infusion Pump" (pump infusion implanted programmable), received between August 2015 and August 2019; the manufacturer given most often on reports is Medtronic Neuromodulation. 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 (84.8%), malfunction (11.4%) and death (3.8%); 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 device operates differently than expected (32.2%), migration or expulsion of device (10%) and material integrity problem (7.1%). The patient problems coded most often are complaint, ill-defined, cerebrospinal fluid leakage and therapeutic response, decreased. 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 Implantable Infusion Pump was received in the five years to August 2026; the latest was received in August 2019.
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 |
|---|---|---|---|
| Device operates differently than expectedthe device behaved unexpectedly | 68 | 32.2% | 8.1% |
| Migration or expulsion of device | 21 | 10% | 5.7% |
| Material integrity problema problem with the device material | 15 | 7.1% | 5.6% |
| Fluid/blood leak | 14 | 6.6% | 2.1% |
| Occlusion within devicethe device blocked | 10 | 4.7% | 1.8% |
| Disconnection | 9 | 4.3% | 1.4% |
| Kinkedthe tube or line kinked | 9 | 4.3% | 1.5% |
| Unstable | 6 | 2.8% | 2.2% |
| Battery problema problem with the battery | 5 | 2.4% | 0.6% |
| Volume accuracy problem | 5 | 2.4% | 4.6% |
| Filling problem | 4 | 1.9% | 2.5% |
| Device displays incorrect message | 3 | 1.4% | 4.5% |
| Device or device fragments location unknown | 3 | 1.4% | 0.6% |
| Aspiration issue | 2 | 0.9% | 2.8% |
| Connection problema connection problem | 2 | 0.9% | 0.2% |
| Improper or incorrect procedure or method | 2 | 0.9% | 4% |
| Malposition of device | 2 | 0.9% | 0.3% |
| Changes in ambient temperature in device environment | 1 | 0.5% | 0% |
| Communication or transmission problemthe device could not communicate or transmit | 1 | 0.5% | 3.9% |
| Difficult to advance | 1 | 0.5% | 0.2% |
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 |
|---|---|---|
| Complaint, ill-defined | 39 | 18.5% |
| Cerebrospinal fluid leakage | 36 | 17.1% |
| Therapeutic response, decreased | 30 | 14.2% |
| Injurya physical injury | 22 | 10.4% |
| Headache, lumbar puncture | 18 | 8.5% |
| Seromaa collection of fluid under the skin | 14 | 6.6% |
| Painpain, site not specified | 13 | 6.2% |
| Therapeutic effects, unexpected | 12 | 5.7% |
| Bacterial infectiona bacterial infection | 11 | 5.2% |
| Muscular rigidity | 9 | 4.3% |
| Wound dehiscencea wound reopened | 9 | 4.3% |
| Muscle spasm(s) | 8 | 3.8% |
| Post operative wound infection | 8 | 3.8% |
| Staphylococcus aureus | 8 | 3.8% |
| Cognitive changes | 6 | 2.8% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Implantable Infusion Pump | Product code LKK | All MAUDE reports |
|---|---|---|---|
| Reports | 211 | 117,271 | 26,136,888 |
| Share of that pool | — | 0.2% | 0% |
| Classified as death, per 1,000 reports | 38 | 14 | 9 |
| Classified as injury | 84.8% | 64% | 36.2% |
| Classified as malfunction | 11.4% | 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% |
| Indura Catheter | 373 | 0 | 0% |
| 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% |
| 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 Implantable Infusion Pump reports
How many FDA reports name Implantable Infusion Pump?
211 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 (84.8%), malfunction (11.4%) and death (3.8%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
device operates differently than expected (32.2%), migration or expulsion of device (10%), material integrity problem (7.1%), fluid/blood leak (6.6%) and occlusion within device (4.7%). 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 Implantable Infusion Pump 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.