Devices › Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (crt-d)
Device brand name · Crt-d
Lumax 540 Hf-T: medical device reports filed with FDA
313 reports name it, 2009–2020. Manufacturer given most often on reports: Biotronik Se & Kg. Product code NIK.
- 313
- device reports naming the brand
- 0% of all MAUDE reports · about 18 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 52.7%
- classified as malfunction
- 47.2% across the product code
- 10.5%
- classified as death, as reported
- 33 reports · not verified by FDA
313 medical device reports received by FDA name the brand "Lumax 540 Hf-T" (crt-d); the manufacturer given most often on reports is Biotronik Se & Kg; received from January 2009 to December 2020. 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 (52.7%), injury (34.5%) and death (10.5%); across all defibrillator, automatic implantable cardioverter, with cardiac resynchronization (crt-d) reports (product code NIK) death is recorded in 2.8% and malfunction in 47.2%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are insufficient device problem information (16.6%), premature elective replacement indicator (13.4%) and inappropriate/inadequate shock/stimulation (12.5%). The patient problems coded most often are shock from patient lead(s), death and hematoma. 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 Lumax 540 Hf-T was received in the five years to August 2026; the latest was received in December 2020.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 170,404 reports carrying product code NIK. 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 |
|---|---|---|---|
| Insufficient device problem information | 52 | 16.6% | 1.3% |
| Premature elective replacement indicator | 42 | 13.4% | 1.4% |
| Inappropriate/inadequate shock/stimulation | 39 | 12.5% | 5.2% |
| Premature end-of-life indicator | 35 | 11.2% | 0.2% |
| Ambient noise problem | 24 | 7.7% | 0.3% |
| Over-sensing | 21 | 6.7% | 22.3% |
| Failure to interrogate | 19 | 6.1% | 2.3% |
| Pacemaker found in back-up mode | 7 | 2.2% | 0.2% |
| High impedance | 6 | 1.9% | 5.6% |
| Explanted | 5 | 1.6% | 0.1% |
| Migration or expulsion of device | 5 | 1.6% | 0.4% |
| Defibrillation/stimulation problem | 4 | 1.3% | 0.7% |
| Device displays incorrect message | 4 | 1.3% | 0.8% |
| Under-sensing | 4 | 1.3% | 1.6% |
| Device remains implanted | 2 | 0.6% | 0% |
| Failure to capture | 2 | 0.6% | 4.1% |
| High capture threshold | 2 | 0.6% | 1% |
| Impedance problem | 2 | 0.6% | 0.5% |
| Normal | 2 | 0.6% | 0.8% |
| Premature discharge of battery | 2 | 0.6% | 11% |
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 |
|---|---|---|
| Shock from patient lead(s) | 50 | 16% |
| Deaththe patient died; cause not stated by this term | 31 | 9.9% |
| Hematomaa collection of blood under the skin or in tissue | 21 | 6.7% |
| Ventricular fibrillationa chaotic rhythm from the lower heart chambers | 8 | 2.6% |
| Painpain, site not specified | 7 | 2.2% |
| Staphylococcus aureus | 7 | 2.2% |
| Surgical procedure | 6 | 1.9% |
| Chest painchest pain | 5 | 1.6% |
| Sepsisa severe body-wide response to infection | 5 | 1.6% |
| Discomfortdiscomfort | 4 | 1.3% |
| Swellingswelling | 4 | 1.3% |
| Cardiac arrestthe heart stopped | 3 | 1% |
| Discharge | 3 | 1% |
| Anemialow red blood cells | 2 | 0.6% |
| Bacterial infectiona bacterial infection | 2 | 0.6% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Lumax 540 Hf-T | Product code NIK | All MAUDE reports |
|---|---|---|---|
| Reports | 313 | 170,404 | 26,136,888 |
| Share of that pool | — | 0.2% | 0% |
| Classified as death, per 1,000 reports | 105 | 28 | 9 |
| Classified as injury | 34.5% | 49.8% | 36.2% |
| Classified as malfunction | 52.7% | 47.2% | 62.3% |
| Filed by the manufacturer | 100% | 99.2% | 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 NIK
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Quadra Assura MP ICD | 14,897 | 507 | 2.1% |
| Gallant HF | 8,971 | 1,918 | 0.7% |
| Quadra Assura Crt-D Quad Rf Hv | 7,971 | 14 | 2.5% |
| Quartet | 14,149 | 848 | 5.2% |
| Unify Assura CRT-D RF HV | 6,731 | 186 | 3.7% |
| Unify Crt-D | 5,907 | 10 | 3.4% |
| Consulta Crt-D | 4,623 | 0 | 5.9% |
| Unify Assura ICD | 4,511 | 127 | 1.6% |
| Claria MRI Quad CRT-D SureScan | 3,775 | 274 | 2.2% |
| Cognis | 8,694 | 6 | 1.5% |
| Protecta Xt Crt-D | 3,541 | 3 | 4.5% |
| Quadra Assura Ddqp+ | 3,349 | 0 | 2.3% |
| Contak Renewal | 3,745 | 0 | 4.8% |
| Cobalt XT HF Quad CRT-D MRI SureScan | 2,581 | 791 | 3% |
| Quadra Assura ICD | 2,526 | 67 | 0.8% |
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 Lumax 540 Hf-T reports
How many FDA reports name Lumax 540 Hf-T?
313 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 (52.7%), injury (34.5%) and death (10.5%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
insufficient device problem information (16.6%), premature elective replacement indicator (13.4%), inappropriate/inadequate shock/stimulation (12.5%), premature end-of-life indicator (11.2%) and ambient noise problem (7.7%). 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 Lumax 540 Hf-T 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.