INTRAMEDULLARY ROD
This device is manufactured by SIGN FRACTURE CARE INTERNATIONAL, SIGN FRACTURE CARE INTL.
The following problems were reported about this device:
Year | Description | Events/year | Type |
---|---|---|---|
2024 | Post Operative Wound Infection | 3 | Patient |
2024 | Limb Fracture | 38 | Patient |
2024 | Break | 5 | Device |
2024 | Adverse Event Without Identified Device or Use Problem | 23 | Device |
2023 | Post Operative Wound Infection | 6 | Patient |
2023 | Limb Fracture | 38 | Patient |
2023 | Migration | 1 | Device |
2023 | Break | 8 | Device |
2023 | Adverse Event Without Identified Device or Use Problem | 22 | Device |
2022 | Limb Fracture | 4 | Patient |
2022 | Positioning Problem | 1 | Device |
2022 | Migration | 1 | Device |
2022 | Break | 9 | Device |
2022 | Adverse Event Without Identified Device or Use Problem | 27 | Device |
2021 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
2019 | Positioning Problem | 1 | Device |
2019 | Migration | 3 | Device |
2019 | Break | 21 | Device |
2019 | Adverse Event Without Identified Device or Use Problem | 95 | Device |
2018 | Migration | 3 | Device |
2018 | Improper or Incorrect Procedure or Method | 1 | Device |
2018 | Break | 43 | Device |
2018 | Adverse Event Without Identified Device or Use Problem | 93 | Device |
2018 | Activation, Positioning or Separation Problem | 1 | Device |
2017 | Unintended Movement | 1 | Device |
2017 | Malposition of Device | 1 | Device |
2017 | Difficult to Insert | 1 | Device |
2017 | Difficult To Position | 1 | Device |
2017 | Break | 29 | Device |
2017 | Adverse Event Without Identified Device or Use Problem | 110 | Device |
2016 | Unintended Movement | 1 | Device |
2016 | Inadequacy of Device Shape and/or Size | 1 | Device |
2016 | Improper or Incorrect Procedure or Method | 1 | Device |
2016 | Device Handling Problem | 18 | Device |
2016 | Break | 40 | Device |
2016 | Adverse Event Without Identified Device or Use Problem | 55 | Device |
2015 | Mechanics Altered | 1 | Device |
2015 | Loose or Intermittent Connection | 1 | Device |
2015 | Fracture | 3 | Device |
2015 | Fitting Problem | 1 | Device |
2015 | Failure to Align | 1 | Device |
2015 | Failure To Adhere Or Bond | 2 | Device |
2015 | Device Operates Differently Than Expected | 1 | Device |
2015 | Break | 11 | Device |
2015 | Appropriate Term/Code Not Available | 1 | Device |
2015 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
2014 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
2013 | Device Handling Problem | 1 | Device |