Devices › System, balloon, intra-aortic and control
Device brand name · System balloon intra-aortic and control
Trans-Ray Plus 7 5 Fr 35cc Iab: medical device reports filed with FDA
344 reports name it, 2017–2023. Manufacturer given most often on reports: Datascope - Fairfield. Product code DSP.
- 344
- device reports naming the brand
- 0% of all MAUDE reports · about 38 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 97.1%
- classified as malfunction
- 89.8% across the product code
- 0.6%
- classified as death, as reported
- 2 reports · not verified by FDA
344 medical device reports received by FDA name the brand "Trans-Ray Plus 7 5 Fr 35cc Iab" (system balloon intra-aortic and control); the manufacturer given most often on reports is Datascope - Fairfield; received from July 2017 to December 2023. 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, 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 (97.1%), injury (2.3%) and death (0.6%); 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 pressure problem (20.6%), leak/splash (18.9%) and optical problem (17.2%). The patient problems coded most often are calcium deposits/calcification, low blood pressure/ hypotension and appropriate clinical signs, symptoms and conditions term/code not available. 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 |
|---|---|---|---|
| Pressure problem | 71 | 20.6% | 1.6% |
| Leak/splashthe device leaked | 65 | 18.9% | 5.5% |
| Optical problem | 59 | 17.2% | 2.1% |
| Difficult to insertthe device was hard to insert | 46 | 13.4% | 3.1% |
| Device displays incorrect message | 24 | 7% | 4.5% |
| Inappropriate waveform | 17 | 4.9% | 0.8% |
| Difficult to advance | 14 | 4.1% | 0.5% |
| Failure to advance | 13 | 3.8% | 0.7% |
| Gas/air leak | 10 | 2.9% | 7.7% |
| Material deformation | 10 | 2.9% | 0.8% |
| Inflation problem | 9 | 2.6% | 3.3% |
| Display or visual feedback problem | 8 | 2.3% | 2.7% |
| Inability to auto-fill | 7 | 2% | 4.3% |
| Unraveled material | 7 | 2% | 0.3% |
| Calibration problem | 6 | 1.7% | 0.8% |
| Migrationthe device moved from where it was placed | 5 | 1.5% | 0.3% |
| Device operates differently than expectedthe device behaved unexpectedly | 4 | 1.2% | 1.6% |
| Difficult to removethe device was hard to remove | 4 | 1.2% | 1% |
| Backflow | 3 | 0.9% | 0.4% |
| Device alarm system | 3 | 0.9% | 2.7% |
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 |
|---|---|---|
| Calcium deposits/calcification | 9 | 2.6% |
| Low blood pressure/ hypotension | 5 | 1.5% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 2 | 0.6% |
| Deaththe patient died; cause not stated by this term | 2 | 0.6% |
| Injurya physical injury | 2 | 0.6% |
| Abdominal painstomach or belly pain | 1 | 0.3% |
| Angina | 1 | 0.3% |
| Bradycardiaslow heart rate | 1 | 0.3% |
| Fecal incontinence | 1 | 0.3% |
| Melena | 1 | 0.3% |
| Myocardial infarctionheart attack | 1 | 0.3% |
| Renal failurekidney failure | 1 | 0.3% |
| Scleroderma | 1 | 0.3% |
| Thrombus | 1 | 0.3% |
| Urinary incontinenceleaking urine | 1 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Trans-Ray Plus 7 5 Fr 35cc Iab | Product code DSP | All MAUDE reports |
|---|---|---|---|
| Reports | 344 | 68,628 | 26,136,888 |
| Share of that pool | — | 0.5% | 0% |
| Classified as death, per 1,000 reports | 6 | 21 | 9 |
| Classified as injury | 2.3% | 7.8% | 36.2% |
| Classified as malfunction | 97.1% | 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 Trans-Ray Plus 7 5 Fr 35cc Iab reports
How many FDA reports name Trans-Ray Plus 7 5 Fr 35cc Iab?
344 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 (97.1%), injury (2.3%) and death (0.6%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
pressure problem (20.6%), leak/splash (18.9%), optical problem (17.2%), difficult to insert (13.4%) and device displays incorrect message (7%). 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 Trans-Ray Plus 7 5 Fr 35cc Iab 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.