Devices › System, balloon, intra-aortic and control
Device brand name · System balloon intra-aortic
Arrow UltraFlex IAB: 7.5Fr 30cc: medical device reports filed with FDA
231 reports name it, 2023–2026. Manufacturer given most often on reports: Arrow International. Product code DSP.
- 231
- device reports naming the brand
- 0% of all MAUDE reports · about 84 a year
- 85
- reports, 12 months to August 2026
- 88 in the 12 months before
- 94.8%
- classified as malfunction
- 89.8% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 231 reports that name the brand "Arrow UltraFlex IAB: 7.5Fr 30cc" (system balloon intra-aortic), received between October 2023 and August 2026; the manufacturer given most often on reports is Arrow International. Spellings of one product vary from report to report.
85 reports arrived in the 12 months to August 2026, close to the 88 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 (94.8%) and injury (5.2%); across all system, balloon, intra-aortic and control reports (product code DSP) death is recorded in 2.1% and malfunction in 89.8%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are patient device interaction problem (19.5%), inflation problem (14.3%) and leak/splash (10%). The patient problems coded most often are cardiogenic shock 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 68,628 reports carrying product code DSP. 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 |
|---|---|---|---|
| Patient device interaction problem | 45 | 19.5% | 0.3% |
| Inflation problem | 33 | 14.3% | 3.3% |
| Leak/splashthe device leaked | 23 | 10% | 5.5% |
| Material deformation | 17 | 7.4% | 0.8% |
| Device alarm system | 15 | 6.5% | 2.7% |
| Material integrity problema problem with the device material | 13 | 5.6% | 0.6% |
| Fluid/blood leak | 11 | 4.8% | 2.4% |
| Material twisted/bent | 11 | 4.8% | 0.3% |
| Material rupture | 8 | 3.5% | 1.3% |
| Entrapment of device | 7 | 3% | 0.3% |
| Obstruction of flow | 5 | 2.2% | 0.6% |
| Difficult to insertthe device was hard to insert | 4 | 1.7% | 3.1% |
| Failure to advance | 3 | 1.3% | 0.7% |
| Material separation | 3 | 1.3% | 0.2% |
| Breakthe device broke | 2 | 0.9% | 2.9% |
| Difficult to advance | 2 | 0.9% | 0.5% |
| Failure to unfold or unwrap | 2 | 0.9% | 0.2% |
| Increase in pressure | 2 | 0.9% | 0.3% |
| Insufficient device problem information | 2 | 0.9% | 0.3% |
| Communication or transmission problemthe device could not communicate or transmit | 1 | 0.4% | 0.7% |
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 |
|---|---|---|
| Cardiogenic shockshock from the heart failing to pump | 1 | 0.4% |
| Foreign body in patientpart of a device left in the patient | 1 | 0.4% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Arrow UltraFlex IAB: 7.5Fr 30cc | Product code DSP | All MAUDE reports |
|---|---|---|---|
| Reports | 231 | 68,628 | 26,136,888 |
| Share of that pool | — | 0.3% | 0% |
| Classified as death, per 1,000 reports | 0 | 21 | 9 |
| Classified as injury | 5.2% | 7.8% | 36.2% |
| Classified as malfunction | 94.8% | 89.8% | 62.3% |
| Filed by the manufacturer | 100% | 96.7% | 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 DSP
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Cardiosave Hybrid Type B Plug | 13,759 | 2,631 | 0.4% |
| Cs300 | 4,197 | 3 | 1.9% |
| CS300 Intra-Aortic Balloon Pump, English, 110V | 2,976 | 466 | 0.3% |
| Cardiosave Hybrid W/ E/F Plug | 1,747 | 402 | 0.3% |
| Cardiosave | 1,673 | 17 | 1.7% |
| System 97 | 1,659 | 0 | 1.7% |
| Cardiosave Hybrid Type I Plug | 1,411 | 485 | 0.1% |
| Sensation Plus 8fr 50cc Iab | 1,368 | 0 | 4.8% |
| Cardiosave Hybrid Type G Plug | 1,342 | 317 | 0.4% |
| Autocat2 Wave | 1,327 | 0 | 1.4% |
| CS300 Intra-Aortic Balloon Pump, English, 220V | 1,146 | 207 | 0.2% |
| Cs100 | 1,012 | 0 | 3.7% |
| SENSATION PLUS 8Fr. 50cc IAB & Accessories (w/Pressure Tubes, No Stylet) | 985 | 491 | 1.4% |
| CS100 Intra-Aortic Balloon Pump, English, 220V | 950 | 159 | 0.4% |
| Stat Dl 9 5 Fr 40 Cc Iab | 907 | 0 | 3% |
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 UltraFlex IAB: 7.5Fr 30cc reports
How many FDA reports name Arrow UltraFlex IAB: 7.5Fr 30cc?
231 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 85 in the latest 12 months.
What kinds of events are reported?
malfunction (94.8%) and injury (5.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
patient device interaction problem (19.5%), inflation problem (14.3%), leak/splash (10%), material deformation (7.4%) and device alarm system (6.5%). 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 Arrow UltraFlex IAB: 7.5Fr 30cc 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.