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This device is manufactured by DAVOL SUB CR BARD.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Skin Inflammation/ Irritation | 1 | Patient |
| 2024 | Pain | 27 | Patient |
| 2024 | Insufficient Information | 128 | Patient |
| 2024 | Patient-Device Incompatibility | 1 | Device |
| 2024 | Patient Device Interaction Problem | 96 | Device |
| 2024 | Insufficient Information | 3 | Device |
| 2024 | Expiration Date Error | 1 | Device |
| 2024 | Device Contamination with Chemical or Other Material | 1 | Device |
| 2024 | Defective Device | 98 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2023 | Pain | 41 | Patient |
| 2023 | Insufficient Information | 121 | Patient |
| 2023 | Patient Device Interaction Problem | 120 | Device |
| 2023 | Insufficient Information | 1 | Device |
| 2023 | Defective Device | 120 | Device |
| 2022 | Pain | 6 | Patient |
| 2022 | Insufficient Information | 6 | Patient |
| 2022 | Patient Device Interaction Problem | 102 | Device |
| 2022 | Device Contamination with Chemical or Other Material | 1 | Device |
| 2022 | Detachment of Device or Device Component | 1 | Device |
| 2022 | Defective Device | 102 | Device |
| 2021 | Pain | 3 | Patient |
| 2021 | Insufficient Information | 3 | Patient |
| 2021 | Patient Device Interaction Problem | 7 | Device |
| 2021 | Insufficient Information | 3 | Device |
| 2021 | Defective Device | 7 | Device |
| 2020 | Pain | 2 | Patient |
| 2020 | Insufficient Information | 2 | Patient |
| 2020 | Patient-Device Incompatibility | 1 | Device |
| 2020 | Patient Device Interaction Problem | 3 | Device |
| 2020 | Defective Device | 4 | Device |