Device brand name · Catheter steerable
G4 Steerable Guiding Catheter Ce: medical device reports filed with FDA
262 reports name it, 2023–2025. Manufacturer given most often on reports: Abbott Medical. Product code DRA.
- 262
- device reports naming the brand
- 0% of all MAUDE reports · about 79 a year
- 2
- reports, 12 months to August 2026
- 43 in the 12 months before
- 51.5%
- classified as malfunction
- 61.9% across the product code
- 1.1%
- classified as death, as reported
- 3 reports · not verified by FDA
262 medical device reports received by FDA name the brand "G4 Steerable Guiding Catheter Ce" (catheter steerable); the manufacturer given most often on reports is Abbott Medical; received from March 2023 to November 2025. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
2 reports arrived in the 12 months to August 2026, down 95% from 43 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 (51.5%), injury (47.3%) and death (1.1%); across all catheter, steerable reports (product code DRA) death is recorded in 1.8% and malfunction in 61.9%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are leak/splash (39.3%), break (8.8%) and material split, cut or torn (6.5%). The patient problems coded most often are perforation, thrombosis/thrombus and air embolism. 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 13,946 reports carrying product code DRA. 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 |
|---|---|---|---|
| Leak/splashthe device leaked | 103 | 39.3% | 16.7% |
| Breakthe device broke | 23 | 8.8% | 1.8% |
| Material split, cut or torn | 17 | 6.5% | 0.7% |
| Improper or incorrect procedure or method | 16 | 6.1% | 0.9% |
| Failure to advance | 13 | 5% | 1.1% |
| Positioning failure | 13 | 5% | 0.9% |
| Deformation due to compressive stress | 12 | 4.6% | 1.4% |
| Difficult to insertthe device was hard to insert | 12 | 4.6% | 1.3% |
| Unintended movement | 8 | 3.1% | 0.8% |
| Difficult to removethe device was hard to remove | 7 | 2.7% | 1.1% |
| Noise, audible | 7 | 2.7% | 0.3% |
| Difficult to advance | 6 | 2.3% | 1.8% |
| Difficult or delayed positioning | 5 | 1.9% | 0.5% |
| Crackthe device cracked | 3 | 1.1% | 0.6% |
| Difficult to flush | 2 | 0.8% | 0.5% |
| Material separation | 2 | 0.8% | 0.2% |
| Physical resistance/sticking | 2 | 0.8% | 0.3% |
| Product quality problem | 2 | 0.8% | 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 |
|---|---|---|
| Perforation | 32 | 12.2% |
| Thrombosis/thrombus | 26 | 9.9% |
| Air embolism | 17 | 6.5% |
| Low blood pressure/ hypotension | 17 | 6.5% |
| Hemorrhage/blood loss/bleeding | 13 | 5% |
| Pericardial effusionfluid around the heart | 11 | 4.2% |
| Hypoxialow oxygen | 10 | 3.8% |
| Cardiac arrestthe heart stopped | 6 | 2.3% |
| Perforation of vessels | 5 | 1.9% |
| Non specific ekg/ECG changes | 4 | 1.5% |
| Cardiac tamponade | 3 | 1.1% |
| Bradycardiaslow heart rate | 2 | 0.8% |
| Cardiogenic shockshock from the heart failing to pump | 2 | 0.8% |
| Embolism/embolus | 2 | 0.8% |
| Hematomaa collection of blood under the skin or in tissue | 2 | 0.8% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | G4 Steerable Guiding Catheter Ce | Product code DRA | All MAUDE reports |
|---|---|---|---|
| Reports | 262 | 13,946 | 26,136,888 |
| Share of that pool | — | 1.9% | 0% |
| Classified as death, per 1,000 reports | 11 | 18 | 9 |
| Classified as injury | 47.3% | 36.2% | 36.2% |
| Classified as malfunction | 51.5% | 61.9% | 62.3% |
| Filed by the manufacturer | 100% | 99.3% | 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 DRA
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| FARADRIVE Steerable Sheath Clear | 4,154 | 1,559 | 0.5% |
| FlexCath Advance Steerable Sheath | 2,941 | 58 | 3.5% |
| Mitraclip System Steerable Guide Catheter | 1,528 | 16 | 3% |
| G4 Steerable Guiding Catheter | 896 | 0 | 1.6% |
| FlexCath Contour Steerable Sheath | 871 | 399 | 1.5% |
| Faradrive | 792 | 192 | 0.9% |
| Mitraclip | 3,357 | 1,161 | 2% |
| Polarsheath | 418 | 12 | 1.2% |
| Flexcath Steerable Sheath | 365 | 0 | 0.3% |
| Steerable Guide Catheter | 336 | 33 | 1.2% |
| FARADRIVE Steerable Sheath | 192 | 102 | 4.2% |
| Mitraclip G4 Steerable Guide Catheter Mdr | 191 | 0 | 1.6% |
| Heartlight | 206 | 0 | 1% |
| Artisan? | 934 | 127 | 0.6% |
| Arctic Front Advance Cardiac Cryoablation Catheter | 2,364 | 46 | 2.6% |
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 G4 Steerable Guiding Catheter Ce reports
How many FDA reports name G4 Steerable Guiding Catheter Ce?
262 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 2 in the latest 12 months.
What kinds of events are reported?
malfunction (51.5%), injury (47.3%) and death (1.1%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
leak/splash (39.3%), break (8.8%), material split, cut or torn (6.5%), improper or incorrect procedure or method (6.1%) and failure to advance (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 G4 Steerable Guiding Catheter Ce 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.