Devices › Catheter, percutaneous
Device brand name · Catheter percutaneous
Guidezilla: medical device reports filed with FDA
1,018 reports name it, 2013–2023. Manufacturer given most often on reports: Boston Scientific - Maple Grove. Product code DQY.
- 1,018
- device reports naming the brand
- 0% of all MAUDE reports · about 79 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 93.9%
- classified as malfunction
- 74.7% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 1,018 reports that name the brand "Guidezilla" (catheter percutaneous), received between August 2013 and February 2023; the manufacturer given most often on reports is Boston Scientific - Maple Grove. 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 malfunction (93.9%) and injury (6%); across all catheter, percutaneous reports (product code DQY) death is recorded in 2.2% and malfunction in 74.7%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are break (35.5%), failure to advance (20.8%) and kinked (10.2%). The patient problems coded most often are no patient involvement, intimal dissection and perforation of vessels. 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 41,793 reports carrying product code DQY. 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 |
|---|---|---|---|
| Breakthe device broke | 361 | 35.5% | 9.2% |
| Failure to advance | 212 | 20.8% | 2.6% |
| Kinkedthe tube or line kinked | 104 | 10.2% | 3.4% |
| Fracturea broken bone | 95 | 9.3% | 2.6% |
| Material deformation | 77 | 7.6% | 5% |
| Difficult to advance | 67 | 6.6% | 1.8% |
| Detachment of device or device componentpart of the device came off | 41 | 4% | 4.6% |
| Detachment of device component | 33 | 3.2% | 2.2% |
| Entrapment of device | 23 | 2.3% | 1.3% |
| Device damaged by another device | 19 | 1.9% | 0.5% |
| Physical resistance | 18 | 1.8% | 1.3% |
| Difficult to removethe device was hard to remove | 16 | 1.6% | 4.1% |
| Material integrity problema problem with the device material | 14 | 1.4% | 2.1% |
| Difficult to insertthe device was hard to insert | 13 | 1.3% | 1.2% |
| Material separation | 9 | 0.9% | 4.1% |
| Device-device incompatibility | 7 | 0.7% | 0.6% |
| Bent | 6 | 0.6% | 0.4% |
| Device damaged prior to usethe device was damaged before use | 6 | 0.6% | 1.8% |
| Compatibility problem | 3 | 0.3% | 0% |
| Defective devicethe device was defective | 3 | 0.3% | 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 |
|---|---|---|
| No patient involvement | 33 | 3.2% |
| Intimal dissection | 13 | 1.3% |
| Perforation of vessels | 4 | 0.4% |
| Vascular dissection | 4 | 0.4% |
| Device embedded in tissue or plaque | 2 | 0.2% |
| Low blood pressure/ hypotension | 2 | 0.2% |
| Heart failure | 1 | 0.1% |
| St segment elevation | 1 | 0.1% |
| Thrombus | 1 | 0.1% |
| Ventricular fibrillationa chaotic rhythm from the lower heart chambers | 1 | 0.1% |
| Ventricular tachycardiaa fast rhythm from the lower heart chambers | 1 | 0.1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Guidezilla | Product code DQY | All MAUDE reports |
|---|---|---|---|
| Reports | 1,018 | 41,793 | 26,136,888 |
| Share of that pool | — | 2.4% | 0% |
| Classified as death, per 1,000 reports | 0 | 22 | 9 |
| Classified as injury | 6% | 22.7% | 36.2% |
| Classified as malfunction | 93.9% | 74.7% | 62.3% |
| Filed by the manufacturer | 99.8% | 97.4% | 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 DQY
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Sterling | 4,963 | 300 | 0.1% |
| Deflect | 1,021 | 247 | 0.1% |
| Lantern Delivery Microcatheter | 887 | 19 | 0% |
| WATCHMAN FXD Curve Access System | 973 | 198 | 9.6% |
| Arrow Cvc Set 2-Lumen 7 Fr X 20 Cm | 1,406 | 170 | 0.1% |
| Coyote? | 1,767 | 122 | 0.1% |
| Advance 35 Lp Low Profile Balloon Catheter | 572 | 15 | 0.5% |
| Conquest Pta Dilatation Catheter | 505 | 0 | 0.2% |
| WATCHMAN TruSeal Access System | 716 | 50 | 8% |
| Sterling Balloon Dilatation Catheter | 488 | 0 | 0.4% |
| React catheter | 516 | 41 | 18.4% |
| Conquest Pta Balloon Dilatation Catheter | 510 | 0 | 0.2% |
| Arrow Cvc Set 3-Lumen 7 Fr X 20 Cm | 1,110 | 123 | 0.1% |
| Neuron Max 6f 088 Long Sheath | 389 | 0 | 0.5% |
| WATCHMAN TruSteer? Access System | 401 | 260 | 9.2% |
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 Guidezilla reports
How many FDA reports name Guidezilla?
1,018 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 (93.9%) and injury (6%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
break (35.5%), failure to advance (20.8%), kinked (10.2%), fracture (9.3%) and material deformation (7.6%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.8%) and voluntary reports (0.1%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Guidezilla 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.