CELLEX PHOTOPHERESIS SYSTEM
This device is manufactured by BECKMAN COULTER, CORDIS CORPORATION, ETHICON ENDO-SURGERY, HOLOGIC, MICROSURGICAL TECHNOLOGY and others.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Fluid/Blood Leak | 24 | Device |
| 2024 | Coagulation in Device or Device Ingredient | 4 | Device |
| 2023 | Granuloma | 1 | Patient |
| 2023 | Fluid/Blood Leak | 14 | Device |
| 2023 | Crack | 1 | Device |
| 2023 | Coagulation in Device or Device Ingredient | 4 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2022 | Hypersensitivity/Allergic reaction | 1 | Patient |
| 2022 | Foreign Body Embolism | 1 | Patient |
| 2022 | Use of Device Problem | 1 | Device |
| 2022 | Unintended Ejection | 1 | Device |
| 2022 | Protective Measures Problem | 1 | Device |
| 2022 | Patient Device Interaction Problem | 1 | Device |
| 2022 | Output Problem | 1 | Device |
| 2022 | Leak/Splash | 2 | Device |
| 2022 | Insufficient Information | 1 | Device |
| 2022 | Improper or Incorrect Procedure or Method | 1 | Device |
| 2022 | Fluid/Blood Leak | 15 | Device |
| 2022 | Coagulation in Device or Device Ingredient | 1 | Device |
| 2022 | Break | 10 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 8 | Device |
| 2021 | Manufacturing, Packaging or Shipping Problem | 1 | Device |