INSTRUMENT
This device is manufactured by DEPUY ORTHOPAEDICS US.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Insufficient Information | 15 | Patient |
| 2024 | Foreign Body In Patient | 3 | Patient |
| 2024 | Naturally Worn | 1 | Device |
| 2024 | Material Deformation | 4 | Device |
| 2024 | Illegible Information | 1 | Device |
| 2024 | Entrapment of Device | 3 | Device |
| 2024 | Crack | 1 | Device |
| 2024 | Break | 36 | Device |
| 2023 | Insufficient Information | 6 | Patient |
| 2023 | Foreign Body In Patient | 1 | Patient |
| 2023 | Material Deformation | 8 | Device |
| 2023 | Illegible Information | 3 | Device |
| 2023 | Failure to Cut | 4 | Device |
| 2023 | Entrapment of Device | 1 | Device |
| 2023 | Break | 34 | Device |
| 2022 | Material Deformation | 8 | Device |
| 2022 | Failure to Cut | 2 | Device |
| 2022 | Entrapment of Device | 1 | Device |
| 2022 | Crack | 1 | Device |
| 2022 | Corroded | 1 | Device |
| 2022 | Break | 26 | Device |
| 2019 | Scratched Material | 1 | Device |
| 2019 | Physical Resistance/Sticking | 1 | Device |
| 2019 | Naturally Worn | 1 | Device |
| 2019 | Material Twisted/Bent | 32 | Device |
| 2019 | Material Fragmentation | 1 | Device |
| 2019 | Entrapment of Device | 2 | Device |
| 2019 | Dull, Blunt | 8 | Device |
| 2019 | Device-Device Incompatibility | 1 | Device |
| 2019 | Deformation Due to Compressive Stress | 2 | Device |
| 2019 | Component Missing | 1 | Device |
| 2019 | Break | 80 | Device |
| 2019 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2018 | Unraveled Material | 2 | Device |
| 2018 | Patient Device Interaction Problem | 2 | Device |
| 2018 | Material Twisted/Bent | 30 | Device |
| 2018 | Material Deformation | 4 | Device |
| 2018 | Insufficient Information | 2 | Device |
| 2018 | Dull, Blunt | 3 | Device |
| 2018 | Defective Device | 1 | Device |
| 2018 | Cut In Material | 1 | Device |
| 2018 | Break | 157 | Device |
| 2018 | Bent | 21 | Device |
| 2018 | Appropriate Term/Code Not Available | 6 | Device |
| 2018 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
| 2017 | Material Twisted/Bent | 1 | Device |
| 2017 | Insufficient Information | 6 | Device |
| 2017 | Fracture | 2 | Device |
| 2017 | Dull, Blunt | 21 | Device |
| 2017 | Disassembly | 1 | Device |
| 2017 | Corroded | 1 | Device |
| 2017 | Break | 146 | Device |
| 2017 | Bent | 42 | Device |
| 2017 | Appropriate Term/Code Not Available | 7 | Device |
| 2016 | Break | 61 | Device |
| 2016 | Bent | 23 | Device |
| 2016 | Appropriate Term/Code Not Available | 1 | Device |
| 2015 | Break | 7 | Device |
| 2015 | Bent | 1 | Device |
| 2015 | Appropriate Term/Code Not Available | 1 | Device |
| 2014 | Break | 9 | Device |