BED, AIR FLUIDIZED
This device is manufactured by HILL ROM, HILL-ROM, HILL-ROM BATESVILLE, MEDTRONIC, MEGADYNE MEDICAL PRODUCTS.
The following problems were reported about this device:
Year | Description | Events/year | Type |
---|---|---|---|
2022 | Hemorrhage/Blood Loss/Bleeding | 7 | Patient |
2022 | Appropriate Term/Code Not Available | 7 | Device |
2015 | Loss of Power | 1 | Device |
2015 | Device Slipped | 1 | Device |
2015 | Device Alarm System | 1 | Device |
2014 | Unintended Movement | 2 | Device |
2014 | Sticking | 1 | Device |
2014 | Sparking | 1 | Device |
2014 | Naturally Worn | 1 | Device |
2014 | Mechanics Altered | 1 | Device |
2014 | Mechanical Problem | 24 | Device |
2014 | Material Protrusion/Extrusion | 1 | Device |
2014 | Malfunction | 1 | Device |
2014 | Lack of Maintenance Documentation or Guidelines | 1 | Device |
2014 | Insufficient Information | 2 | Device |
2014 | Inflation Problem | 1 | Device |
2014 | Incorrect Device Or Component Shipped | 1 | Device |
2014 | Improper Flow or Infusion | 1 | Device |
2014 | Display or Visual Feedback Problem | 1 | Device |
2014 | Device Slipped | 176 | Device |
2014 | Device Operates Differently Than Expected | 7 | Device |
2014 | Device Inoperable | 2 | Device |
2014 | Device Displays Incorrect Message | 1 | Device |
2014 | Device Alarm System | 1 | Device |
2014 | Collapse | 1 | Device |
2014 | Break | 4 | Device |
2014 | Application Interface Becomes Non-Functional Or Program Exits Abnormally | 1 | Device |
2013 | Unintended Head Motion | 1 | Device |
2013 | Thermal Decomposition of Device | 1 | Device |
2013 | Leak/Splash | 1 | Device |
2013 | Improper or Incorrect Procedure or Method | 1 | Device |
2013 | Fire | 1 | Device |
2013 | Device Slipped | 18 | Device |
2013 | Device Operates Differently Than Expected | 1 | Device |