87JDI; 87LPH
This device is manufactured by DEPUY, DEPUY FRANCE SAS - 3003895575, DEPUY INTERNATIONAL, DEPUY INTL - 8010379, DEPUY IRELAND - 9616671 and others.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Unspecified Infection | 1 | Patient |
| 2024 | Pain | 3 | Patient |
| 2024 | Insufficient Information | 1 | Patient |
| 2024 | Adverse Event Without Identified Device or Use Problem | 4 | Device |
| 2023 | Unspecified Infection | 2 | Patient |
| 2023 | Pain | 6 | Patient |
| 2023 | Metal Related Pathology | 1 | Patient |
| 2023 | Joint Laxity | 1 | Patient |
| 2023 | Joint Dislocation | 1 | Patient |
| 2023 | Insufficient Information | 1 | Patient |
| 2023 | Hematoma | 1 | Patient |
| 2023 | Fall | 1 | Patient |
| 2023 | No Apparent Adverse Event | 1 | Device |
| 2023 | Naturally Worn | 1 | Device |
| 2023 | Device Dislodged or Dislocated | 1 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 8 | Device |
| 2022 | Pain | 1 | Patient |
| 2022 | Joint Dislocation | 2 | Patient |
| 2022 | Device Dislodged or Dislocated | 3 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 4 | Device |
| 2021 | Swelling/ Edema | 1 | Patient |
| 2021 | Scar Tissue | 1 | Patient |
| 2021 | Pain | 1 | Patient |
| 2021 | Metal Related Pathology | 1 | Patient |
| 2021 | Loss of Range of Motion | 1 | Patient |
| 2021 | Inflammation | 1 | Patient |
| 2021 | Hypersensitivity/Allergic reaction | 1 | Patient |
| 2021 | Foreign Body Reaction | 1 | Patient |
| 2021 | Distress | 1 | Patient |
| 2021 | Adhesion(s) | 1 | Patient |
| 2021 | Naturally Worn | 1 | Device |
| 2020 | Naturally Worn | 1 | Device |
| 2020 | Device Dislodged or Dislocated | 1 | Device |
| 2020 | Appropriate Term/Code Not Available | 1 | Device |