Devices › Catheter, percutaneous
Device brand name · Catheter percutaneous
Arrow Arterial Cath Set 20 Ga X 8cm: medical device reports filed with FDA
305 reports name it, 2018–2026. Manufacturer given most often on reports: Arrow International. Product code DQY.
- 305
- device reports naming the brand
- 0% of all MAUDE reports · about 39 a year
- 61
- reports, 12 months to August 2026
- 71 in the 12 months before
- 96.1%
- 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 305 reports that name the brand "Arrow Arterial Cath Set 20 Ga X 8cm" (catheter percutaneous), received between August 2018 and August 2026; the manufacturer given most often on reports is Arrow International. Spellings of one product vary from report to report.
61 reports arrived in the 12 months to August 2026, down 14% from 71 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 (96.1%) and injury (3.9%); 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 material twisted/bent (33.4%), material separation (18%) and incorrect, inadequate or imprecise result or readings (12.8%). The patient problems coded most often are ischemia, swelling/ edema and foreign body in patient. 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 |
|---|---|---|---|
| Material twisted/bent | 102 | 33.4% | 2.4% |
| Material separation | 55 | 18% | 4.1% |
| Incorrect, inadequate or imprecise result or readings | 39 | 12.8% | 0.3% |
| Breakthe device broke | 37 | 12.1% | 9.2% |
| Deformation due to compressive stress | 27 | 8.9% | 2.3% |
| Unable to obtain readings | 24 | 7.9% | 0.3% |
| Device damaged prior to usethe device was damaged before use | 18 | 5.9% | 1.8% |
| Failure to obtain sample | 16 | 5.2% | 0.1% |
| Obstruction of flow | 13 | 4.3% | 0.6% |
| Pressure problem | 7 | 2.3% | 0% |
| Insufficient device problem information | 6 | 2% | 0.9% |
| Physical resistance/sticking | 6 | 2% | 2.9% |
| Biocompatibility | 5 | 1.6% | 0.1% |
| No flow | 5 | 1.6% | 0.1% |
| Patient device interaction problem | 5 | 1.6% | 0.2% |
| Device displays incorrect message | 3 | 1% | 0% |
| Incorrect measurementthe device measured wrongly | 2 | 0.7% | 0% |
| Material deformation | 2 | 0.7% | 5% |
| Material integrity problema problem with the device material | 2 | 0.7% | 2.1% |
| Difficult to removethe device was hard to remove | 1 | 0.3% | 4.1% |
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 |
|---|---|---|
| Ischemia | 9 | 3% |
| Swelling/ edema | 7 | 2.3% |
| Foreign body in patientpart of a device left in the patient | 6 | 2% |
| Hematomaa collection of blood under the skin or in tissue | 6 | 2% |
| Needle stick/puncture | 6 | 2% |
| Reduced blood flow | 6 | 2% |
| Thrombosis/thrombus | 6 | 2% |
| Discomfortdiscomfort | 4 | 1.3% |
| Painpain, site not specified | 4 | 1.3% |
| High blood pressure/ hypertension | 2 | 0.7% |
| Skin discoloration | 2 | 0.7% |
| Blistera blister | 1 | 0.3% |
| Easy bruising | 1 | 0.3% |
| Numbnessnumbness | 1 | 0.3% |
| Vascular dissection | 1 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Arrow Arterial Cath Set 20 Ga X 8cm | Product code DQY | All MAUDE reports |
|---|---|---|---|
| Reports | 305 | 41,793 | 26,136,888 |
| Share of that pool | — | 0.7% | 0% |
| Classified as death, per 1,000 reports | 0 | 22 | 9 |
| Classified as injury | 3.9% | 22.7% | 36.2% |
| Classified as malfunction | 96.1% | 74.7% | 62.3% |
| Filed by the manufacturer | 100% | 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% |
| Guidezilla | 1,018 | 0 | 0% |
| 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% |
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 Arrow Arterial Cath Set 20 Ga X 8cm reports
How many FDA reports name Arrow Arterial Cath Set 20 Ga X 8cm?
305 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 61 in the latest 12 months.
What kinds of events are reported?
malfunction (96.1%) and injury (3.9%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
material twisted/bent (33.4%), material separation (18%), incorrect, inadequate or imprecise result or readings (12.8%), break (12.1%) and deformation due to compressive stress (8.9%). 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 Arrow Arterial Cath Set 20 Ga X 8cm 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.