Devices › System, balloon, intra-aortic and control
Device brand name · System balloon intra-aortic
Ultraflex Iab 7 5fr 40cc: medical device reports filed with FDA
362 reports name it, 2015–2024. Manufacturer given most often on reports: Arrow International. Product code DSP.
- 362
- device reports naming the brand
- 0% of all MAUDE reports · about 33 a year
- 0
- reports, 12 months to August 2026
- 1 in the 12 months before
- 84.3%
- classified as malfunction
- 89.8% across the product code
- 2.2%
- classified as death, as reported
- 8 reports · not verified by FDA
362 medical device reports received by FDA name the brand "Ultraflex Iab 7 5fr 40cc" (system balloon intra-aortic); the manufacturer given most often on reports is Arrow International; received from September 2015 to November 2024. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
0 reports arrived in the 12 months to August 2026, against 1 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 (84.3%), injury (13.5%) and death (2.2%); 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 fluid/blood leak (31.2%), gas/air leak (11.6%) and material rupture (10.2%). The patient problems coded most often are needle stick/puncture, death and myocardial infarction. 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 |
|---|---|---|---|
| Fluid/blood leak | 113 | 31.2% | 2.4% |
| Gas/air leak | 42 | 11.6% | 7.7% |
| Material rupture | 37 | 10.2% | 1.3% |
| Inflation problem | 32 | 8.8% | 3.3% |
| Difficult to insertthe device was hard to insert | 20 | 5.5% | 3.1% |
| Leak/splashthe device leaked | 20 | 5.5% | 5.5% |
| Device alarm system | 17 | 4.7% | 2.7% |
| Difficult to advance | 15 | 4.1% | 0.5% |
| Breakthe device broke | 14 | 3.9% | 2.9% |
| Deformation due to compressive stress | 12 | 3.3% | 0.1% |
| Material twisted/bent | 10 | 2.8% | 0.3% |
| Material integrity problema problem with the device material | 8 | 2.2% | 0.6% |
| Failure to advance | 7 | 1.9% | 0.7% |
| Complete blockage | 5 | 1.4% | 0.1% |
| Difficult to removethe device was hard to remove | 4 | 1.1% | 1% |
| Fracturea broken bone | 4 | 1.1% | 0.2% |
| Kinkedthe tube or line kinked | 4 | 1.1% | 0.5% |
| Burst container or vessel | 3 | 0.8% | 0% |
| Defective devicethe device was defective | 3 | 0.8% | 0.2% |
| Difficult to flush | 3 | 0.8% | 0.3% |
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 |
|---|---|---|
| Needle stick/puncture | 16 | 4.4% |
| Deaththe patient died; cause not stated by this term | 14 | 3.9% |
| Myocardial infarctionheart attack | 6 | 1.7% |
| Blood loss | 5 | 1.4% |
| Calcium deposits/calcification | 5 | 1.4% |
| Cardiogenic shockshock from the heart failing to pump | 5 | 1.4% |
| Low blood pressure/ hypotension | 5 | 1.4% |
| Cardiac arrestthe heart stopped | 4 | 1.1% |
| Atrial fibrillationan irregular heart rhythm | 2 | 0.6% |
| Cardiomyopathydisease of the heart muscle | 2 | 0.6% |
| Device embedded in tissue or plaque | 2 | 0.6% |
| Heart failure | 2 | 0.6% |
| Ischemia | 2 | 0.6% |
| Respiratory failurethe lungs could not supply enough oxygen | 2 | 0.6% |
| Vascular dissection | 2 | 0.6% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Ultraflex Iab 7 5fr 40cc | Product code DSP | All MAUDE reports |
|---|---|---|---|
| Reports | 362 | 68,628 | 26,136,888 |
| Share of that pool | — | 0.5% | 0% |
| Classified as death, per 1,000 reports | 22 | 21 | 9 |
| Classified as injury | 13.5% | 7.8% | 36.2% |
| Classified as malfunction | 84.3% | 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 Ultraflex Iab 7 5fr 40cc reports
How many FDA reports name Ultraflex Iab 7 5fr 40cc?
362 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 (84.3%), injury (13.5%) and death (2.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
fluid/blood leak (31.2%), gas/air leak (11.6%), material rupture (10.2%), inflation problem (8.8%) and difficult to insert (5.5%). 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 Ultraflex Iab 7 5fr 40cc 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.