Devices › Ventricular (assist) bypass
Device brand name · Ventricular assist bypass
Thoratec HeartMate 3 VAD Modular Cable: medical device reports filed with FDA
657 reports name it, 2023–2026. Manufacturer given most often on reports: Thoratec. Product code DSQ.
- 657
- device reports naming the brand
- 0% of all MAUDE reports · about 239 a year
- 251
- reports, 12 months to August 2026
- 261 in the 12 months before
- 93.5%
- classified as malfunction
- 37% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
657 medical device reports received by FDA name the brand "Thoratec HeartMate 3 VAD Modular Cable" (ventricular assist bypass); the manufacturer given most often on reports is Thoratec; received from October 2023 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
251 reports arrived in the 12 months to August 2026, close to the 261 of 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 (93.5%) and injury (6.5%); across all ventricular (assist) bypass reports (product code DSQ) death is recorded in 14.6% and malfunction in 37%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are mechanical problem (39.7%), electrical /electronic property problem (33.8%) and communication or transmission problem (18.9%). The patient problems coded most often are anxiety, presyncope and burn(s). 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 158,083 reports carrying product code DSQ. 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 |
|---|---|---|---|
| Mechanical problema mechanical problem | 261 | 39.7% | 5.5% |
| Electrical /electronic property probleman electrical or electronic problem | 222 | 33.8% | 1.9% |
| Communication or transmission problemthe device could not communicate or transmit | 124 | 18.9% | 0.8% |
| Corrodedthe device corroded | 58 | 8.8% | 0.2% |
| Insufficient device problem information | 49 | 7.5% | 1.8% |
| Device difficult to setup or prepare | 28 | 4.3% | 0.6% |
| Contamination /decontamination problem | 23 | 3.5% | 0.1% |
| Material twisted/bent | 21 | 3.2% | 1% |
| Disconnection | 16 | 2.4% | 2% |
| Material discolored | 8 | 1.2% | 0.1% |
| Premature separation | 7 | 1.1% | 0% |
| Separation failure | 7 | 1.1% | 0% |
| Electrical power problem | 6 | 0.9% | 2.1% |
| Unintended electrical shock | 4 | 0.6% | 0.1% |
| Loose or intermittent connection | 2 | 0.3% | 0.9% |
| Manufacturing, packaging or shipping problem | 2 | 0.3% | 0% |
| Data problem | 1 | 0.2% | 0.2% |
| Improper or incorrect procedure or method | 1 | 0.2% | 0.5% |
| Overheating of device | 1 | 0.2% | 0.3% |
| Pumping stopped | 1 | 0.2% | 3.2% |
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 |
|---|---|---|
| Anxietyanxiety | 2 | 0.3% |
| Presyncope | 2 | 0.3% |
| Burn(s)a burn | 1 | 0.2% |
| Discomfortdiscomfort | 1 | 0.2% |
| Dyspneashortness of breath | 1 | 0.2% |
| Falla fall | 1 | 0.2% |
| Hemodynamic instability | 1 | 0.2% |
| Loss of consciousnesspassing out | 1 | 0.2% |
| Low blood pressure/ hypotension | 1 | 0.2% |
| Shock from patient lead(s) | 1 | 0.2% |
| Syncope/fainting | 1 | 0.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Thoratec HeartMate 3 VAD Modular Cable | Product code DSQ | All MAUDE reports |
|---|---|---|---|
| Reports | 657 | 158,083 | 26,136,888 |
| Share of that pool | — | 0.4% | 0% |
| Classified as death, per 1,000 reports | 0 | 146 | 9 |
| Classified as injury | 6.5% | 48.3% | 36.2% |
| Classified as malfunction | 93.5% | 37% | 62.3% |
| Filed by the manufacturer | 100% | 97% | 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 DSQ
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| HeartWare Ventricular Assist System - Pump | 36,450 | 1,304 | 13.4% |
| Heartware Ventricular Assist System | 14,550 | 0 | 6.9% |
| HeartMate 3 LVAS Implant Kit | 13,500 | 626 | 38% |
| Thoratec HeartMate 3 LVAS Implant Kit | 8,130 | 3,008 | 29.7% |
| HeartMate 3 Left Ventricular Assist System | 5,858 | 122 | 18.6% |
| HeartWare Ventricular Assist System - Controller 2.0 | 5,831 | 132 | 0.5% |
| HeartWare Ventricular Assist System - Battery | 5,010 | 47 | 0% |
| Thoratec HeartMate 3 System Controller | 3,591 | 1,387 | 0% |
| HeartMate 3 System Controller | 3,473 | 247 | 0.3% |
| HeartWare Ventricular Assist System - Driveline | 3,003 | 159 | 1.5% |
| HeartWare Ventricular Assist System - Pump/Driveline | 2,160 | 147 | 16.6% |
| Heartmate Mobile Power Unit Na | 2,096 | 4 | 0.1% |
| Heartware Ventricular Assist System-Pump | 1,424 | 0 | 19.9% |
| Heartware Ventricular Assist System- Pump | 1,306 | 0 | 35.4% |
| Heartmate Mobile Power Unit N/A | 1,234 | 519 | 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 Thoratec HeartMate 3 VAD Modular Cable reports
How many FDA reports name Thoratec HeartMate 3 VAD Modular Cable?
657 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 251 in the latest 12 months.
What kinds of events are reported?
malfunction (93.5%) and injury (6.5%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
mechanical problem (39.7%), electrical /electronic property problem (33.8%), communication or transmission problem (18.9%), corroded (8.8%) and insufficient device problem information (7.5%). 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 Thoratec HeartMate 3 VAD Modular Cable 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.