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This device is manufactured by BARD DAVOL, DAVOL SUB CR BARD.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Pain | 32 | Patient |
| 2024 | Insufficient Information | 185 | Patient |
| 2024 | Patient-Device Incompatibility | 5 | Device |
| 2024 | Patient Device Interaction Problem | 156 | Device |
| 2024 | Defective Device | 156 | Device |
| 2023 | Unspecified Infection | 1 | Patient |
| 2023 | Sepsis | 1 | Patient |
| 2023 | Scar Tissue | 1 | Patient |
| 2023 | Pain | 54 | Patient |
| 2023 | Insufficient Information | 149 | Patient |
| 2023 | Hypersensitivity/Allergic reaction | 1 | Patient |
| 2023 | Hematoma | 1 | Patient |
| 2023 | Bowel Perforation | 1 | Patient |
| 2023 | Patient-Device Incompatibility | 2 | Device |
| 2023 | Patient Device Interaction Problem | 144 | Device |
| 2023 | No Apparent Adverse Event | 2 | Device |
| 2023 | Insufficient Information | 2 | Device |
| 2023 | Defective Device | 146 | Device |
| 2022 | Pain | 1 | Patient |
| 2022 | Insufficient Information | 1 | Patient |
| 2022 | Patient Device Interaction Problem | 112 | Device |
| 2022 | Defective Device | 112 | Device |
| 2021 | Pain | 1 | Patient |
| 2021 | Insufficient Information | 1 | Patient |
| 2021 | Patient Device Interaction Problem | 3 | Device |
| 2021 | Insufficient Information | 1 | Device |
| 2021 | Defective Device | 3 | Device |
| 2020 | Pain | 2 | Patient |
| 2020 | Insufficient Information | 2 | Patient |
| 2020 | Patient Device Interaction Problem | 2 | Device |
| 2020 | Defective Device | 2 | Device |