27.5 TRANSVERSE CONNECTOR
This device is manufactured by BOSTON SCIENTIFIC CORPORATION.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Vascular Dissection | 19 | Patient |
| 2024 | Restenosis | 4 | Patient |
| 2024 | Reduced Blood Flow | 11 | Patient |
| 2024 | Non specific EKG/ECG Changes | 1 | Patient |
| 2024 | Nausea | 2 | Patient |
| 2024 | Low Blood Pressure/ Hypotension | 1 | Patient |
| 2024 | Ischemia | 1 | Patient |
| 2024 | Insufficient Information | 2 | Patient |
| 2024 | High Blood Pressure/ Hypertension | 2 | Patient |
| 2024 | Foreign Body In Patient | 1 | Patient |
| 2024 | Discomfort | 3 | Patient |
| 2024 | Diaphoresis | 2 | Patient |
| 2024 | Chest Pain | 2 | Patient |
| 2024 | Cardiogenic Shock | 1 | Patient |
| 2024 | Cardiac Arrest | 2 | Patient |
| 2024 | Arteriosclerosis/ Atherosclerosis | 1 | Patient |
| 2024 | Angina | 8 | Patient |
| 2024 | Material Deformation | 4 | Device |
| 2024 | Inflation Problem | 1 | Device |
| 2024 | Fracture | 2 | Device |
| 2024 | Failure to Deflate | 1 | Device |
| 2024 | Failure to Advance | 2 | Device |
| 2024 | Difficult to Advance | 4 | Device |
| 2024 | Device-Device Incompatibility | 1 | Device |
| 2024 | Device Dislodged or Dislocated | 5 | Device |
| 2024 | Device Damaged by Another Device | 1 | Device |
| 2024 | Break | 5 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 21 | Device |
| 2024 | Activation Failure | 1 | Device |
| 2023 | Vascular Dissection | 22 | Patient |
| 2023 | Thrombosis/Thrombus | 4 | Patient |
| 2023 | Restenosis | 5 | Patient |
| 2023 | Reduced Blood Flow | 7 | Patient |
| 2023 | Perforation | 1 | Patient |
| 2023 | Non specific EKG/ECG Changes | 1 | Patient |
| 2023 | Myocardial Infarction | 1 | Patient |
| 2023 | Ischemia | 3 | Patient |
| 2023 | Hematoma | 1 | Patient |
| 2023 | Heart Failure/Congestive Heart Failure | 3 | Patient |
| 2023 | Foreign Body In Patient | 1 | Patient |
| 2023 | Chest Pain | 4 | Patient |
| 2023 | Cardiomyopathy | 1 | Patient |
| 2023 | Cardiac Arrest | 3 | Patient |
| 2023 | Arteriosclerosis/ Atherosclerosis | 6 | Patient |
| 2023 | Angina | 18 | Patient |
| 2023 | Positioning Problem | 1 | Device |
| 2023 | Obstruction of Flow | 3 | Device |
| 2023 | Material Rupture | 3 | Device |
| 2023 | Material Integrity Problem | 1 | Device |
| 2023 | Material Deformation | 7 | Device |
| 2023 | Fracture | 5 | Device |
| 2023 | Failure to Deflate | 2 | Device |
| 2023 | Failure to Advance | 8 | Device |
| 2023 | Entrapment of Device | 2 | Device |
| 2023 | Difficult to Remove | 3 | Device |
| 2023 | Difficult to Advance | 4 | Device |
| 2023 | Device Dislodged or Dislocated | 6 | Device |
| 2023 | Device Damaged by Another Device | 2 | Device |
| 2023 | Break | 8 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 53 | Device |
| 2022 | Vascular Dissection | 1 | Patient |
| 2022 | Restenosis | 9 | Patient |
| 2022 | Myocardial Infarction | 1 | Patient |
| 2022 | Ischemia | 1 | Patient |
| 2022 | Heart Failure/Congestive Heart Failure | 2 | Patient |
| 2022 | Fatigue | 1 | Patient |
| 2022 | Dyspnea | 2 | Patient |
| 2022 | Cardiac Enzyme Elevation | 1 | Patient |
| 2022 | Angina | 8 | Patient |
| 2022 | Positioning Problem | 1 | Device |
| 2022 | Obstruction of Flow | 5 | Device |
| 2022 | Material Rupture | 1 | Device |
| 2022 | Material Integrity Problem | 1 | Device |
| 2022 | Material Deformation | 32 | Device |
| 2022 | Fracture | 2 | Device |
| 2022 | Failure to Advance | 32 | Device |
| 2022 | Difficult to Remove | 4 | Device |
| 2022 | Difficult to Advance | 6 | Device |
| 2022 | Difficult or Delayed Positioning | 1 | Device |
| 2022 | Device Markings/Labelling Problem | 1 | Device |
| 2022 | Device Dislodged or Dislocated | 3 | Device |
| 2022 | Device Damaged by Another Device | 3 | Device |
| 2022 | Deflation Problem | 1 | Device |
| 2022 | Defective Device | 4 | Device |
| 2022 | Break | 15 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 28 | Device |
| 2022 | Activation Failure | 4 | Device |
| 2021 | Thrombosis/Thrombus | 3 | Patient |
| 2021 | Restenosis | 5 | Patient |
| 2021 | Heart Failure/Congestive Heart Failure | 1 | Patient |
| 2021 | Arteriosclerosis/ Atherosclerosis | 1 | Patient |
| 2021 | Angina | 6 | Patient |
| 2021 | Failure to Advance | 8 | Device |
| 2021 | Adverse Event Without Identified Device or Use Problem | 11 | Device |
| 2020 | Restenosis | 1 | Patient |
| 2020 | Ischemic Heart Disease | 2 | Patient |
| 2020 | Hypokalemia | 2 | Patient |
| 2020 | Fever | 2 | Patient |
| 2020 | Arteriosclerosis/ Atherosclerosis | 1 | Patient |
| 2020 | Angina | 2 | Patient |
| 2020 | Anemia | 2 | Patient |
| 2020 | Material Deformation | 1 | Device |
| 2020 | Adverse Event Without Identified Device or Use Problem | 7 | Device |