87LXH
This device is manufactured by DEPUY FRANCE SAS - 3003895575, DEPUY INTERNATIONAL, DEPUY ORTHOPAEDICS 1818910DEPUY ORTHOPAEDICS, DEPUY ORTHOPAEDICS US.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Insufficient Information | 37 | Patient |
| 2024 | Unintended Movement | 2 | Device |
| 2024 | No Apparent Adverse Event | 2 | Device |
| 2024 | Naturally Worn | 13 | Device |
| 2024 | Material Deformation | 1 | Device |
| 2024 | Device-Device Incompatibility | 5 | Device |
| 2024 | Crack | 2 | Device |
| 2024 | Break | 86 | Device |
| 2023 | Insufficient Information | 13 | Patient |
| 2023 | Unintended Movement | 1 | Device |
| 2023 | Scratched Material | 2 | Device |
| 2023 | Naturally Worn | 20 | Device |
| 2023 | Material Integrity Problem | 2 | Device |
| 2023 | Material Deformation | 1 | Device |
| 2023 | Device-Device Incompatibility | 4 | Device |
| 2023 | Crack | 2 | Device |
| 2023 | Break | 127 | Device |
| 2022 | No Apparent Adverse Event | 5 | Device |
| 2022 | Naturally Worn | 8 | Device |
| 2022 | Material Integrity Problem | 1 | Device |
| 2022 | Material Deformation | 1 | Device |
| 2022 | Entrapment of Device | 1 | Device |
| 2022 | Device-Device Incompatibility | 2 | Device |
| 2022 | Crack | 4 | Device |
| 2022 | Break | 126 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2021 | Break | 1 | Device |
| 2020 | Break | 1 | Device |