MGB
This device is manufactured by ACCESSCLOSURE, ACCESSCLOSURE A CARDINAL HEALTH COMPANY, CARDINAL HEALTH, CARDINAL HEALTH SANTA CLARA, CORDIS CORPORATION.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2023 | Separation Failure | 1 | Device |
| 2023 | Migration | 2 | Device |
| 2023 | Failure to Advance | 1 | Device |
| 2023 | Entrapment of Device | 2 | Device |
| 2023 | Difficult to Remove | 2 | Device |
| 2023 | Deflation Problem | 1 | Device |
| 2023 | Defective Component | 3 | Device |
| 2022 | Therapy Delivered to Incorrect Body Area | 1 | Device |
| 2022 | Separation Failure | 1 | Device |
| 2022 | Retraction Problem | 1 | Device |
| 2022 | Positioning Failure | 2 | Device |
| 2022 | Migration | 3 | Device |
| 2022 | Material Rupture | 3 | Device |
| 2022 | Material Puncture/Hole | 5 | Device |
| 2022 | Failure to Advance | 2 | Device |
| 2022 | Difficult to Advance | 1 | Device |
| 2022 | Difficult or Delayed Positioning | 2 | Device |
| 2022 | Device Damaged by Another Device | 1 | Device |
| 2022 | Detachment of Device or Device Component | 2 | Device |
| 2022 | Deflation Problem | 1 | Device |
| 2022 | Decrease in Pressure | 9 | Device |
| 2022 | Appropriate Term/Code Not Available | 2 | Device |
| 2022 | Activation, Positioning or Separation Problem | 1 | Device |