87KWA
This device is manufactured by DEPUY INTERNATIONAL, DEPUY INTL - 8010379, DEPUY ORTHOPAEDICS US.
The following problems were reported about this device:
Year | Description | Events/year | Type |
---|---|---|---|
2024 | Pain | 1 | Patient |
2024 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
2023 | Pain | 1 | Patient |
2023 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
2022 | Unspecified Infection | 3 | Patient |
2022 | Synovitis | 1 | Patient |
2022 | Sepsis | 1 | Patient |
2022 | Pain | 1 | Patient |
2022 | Low Blood Pressure/ Hypotension | 1 | Patient |
2022 | Cyst(s) | 1 | Patient |
2022 | Device Dislodged or Dislocated | 1 | Device |
2022 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
2021 | Synovitis | 1 | Patient |
2021 | Metal Related Pathology | 1 | Patient |
2021 | Insufficient Information | 1 | Patient |
2021 | Foreign Body Reaction | 1 | Patient |
2021 | Naturally Worn | 1 | Device |
2021 | Adverse Event Without Identified Device or Use Problem | 1 | Device |