POWER PRO AMBULANCE COT

PUMP, INFUSION

This device is manufactured by STRYKER MEDICAL-KALAMAZOO.

The following problems were reported about this device:

Year Description Events/year Type
2023 Unspecified Musculoskeletal problem 1 Patient
2023 Muscle/Tendon Damage 1 Patient
2023 Insufficient Information 3 Patient
2023 Positioning Failure 2 Device
2023 Difficult to Remove 2 Device
2023 Difficult or Delayed Positioning 2 Device
2023 Device Dislodged or Dislocated 1 Device
2022 Sharp Edges 2 Device
2022 Protective Measures Problem 3 Device
2022 Positioning Failure 8 Device
2022 Difficult to Remove 7 Device
2022 Difficult or Delayed Positioning 8 Device
2022 Device Tipped Over 5 Device
2022 Device Fell 4 Device
2022 Device Dislodged or Dislocated 4 Device
2019 Unintended Movement 2 Device
2019 Therapeutic or Diagnostic Output Failure 2 Device
2019 Sharp Edges 2 Device
2019 Positioning Failure 3 Device
2019 Patient Device Interaction Problem 1 Device
2019 Misassembled During Installation 1 Device
2019 Misassembled 1 Device
2019 Mechanical Problem 1 Device
2019 Difficult to Remove 1 Device
2019 Difficult or Delayed Positioning 2 Device
2019 Device Tipped Over 4 Device
2019 Device Slipped 2 Device
2019 Device Fell 7 Device
2019 Device Dislodged or Dislocated 1 Device
2019 Detachment of Device or Device Component 1 Device
2019 Component Missing 1 Device
2018 Unstable 1 Device
2018 Unintended Movement 1 Device
2018 Sharp Edges 1 Device
2018 Positioning Failure 4 Device
2018 Mechanical Jam 4 Device
2018 Improper or Incorrect Procedure or Method 2 Device
2018 Difficult to Remove 1 Device
2018 Difficult to Advance 1 Device
2018 Difficult or Delayed Positioning 9 Device
2018 Device Tipped Over 10 Device
2018 Device Operates Differently Than Expected 1 Device
2018 Device Fell 4 Device
2018 Component Falling 2 Device
2018 Break 1 Device
2018 Adverse Event Without Identified Device or Use Problem 1 Device
2017 Use of Device Problem 1 Device
2017 Unintended System Motion 1 Device
2017 Unintended Movement 6 Device
2017 Unintended Collision 1 Device
2017 Positioning Problem 5 Device
2017 Noise, Audible 1 Device
2017 Mechanical Problem 5 Device
2017 Material Protrusion/Extrusion 2 Device
2017 Malposition of Device 1 Device
2017 Loose or Intermittent Connection 1 Device
2017 Insufficient Information 4 Device
2017 Improper or Incorrect Procedure or Method 3 Device
2017 Device Tipped Over 4 Device
2017 Device Operates Differently Than Expected 4 Device
2017 Detachment Of Device Component 2 Device
2017 Component Falling 3 Device
2017 Break 2 Device
2017 Bent 1 Device
2017 Adverse Event Without Identified Device or Use Problem 4 Device
2016 Use of Device Problem 1 Device
2016 Unintended System Motion 1 Device
2016 Unintended Collision 1 Device
2016 Protective Measures Problem 2 Device
2016 Mechanics Altered 1 Device
2016 Malposition of Device 1 Device
2016 Insufficient Information 1 Device
2016 Improper or Incorrect Procedure or Method 1 Device
2016 Fail-Safe Design Failure 1 Device
2016 Device Tipped Over 3 Device
2016 Device Slipped 1 Device
2016 Component Missing 1 Device
2016 Component Falling 1 Device
2016 Adverse Event Without Identified Device or Use Problem 2 Device
2015 Fail-Safe Design Failure 1 Device
2015 Device Tipped Over 1 Device
2015 Adverse Event Without Identified Device or Use Problem 1 Device
2014 Unintended Head Motion 1 Device
2014 Sticking 6 Device
2014 Smoking 2 Device
2014 Scratched Material 1 Device
2014 Positioning Problem 2 Device
2014 Naturally Worn 2 Device
2014 Mechanical Jam 1 Device
2014 Material Integrity Problem 1 Device
2014 Loose or Intermittent Connection 1 Device
2014 Kinked 1 Device
2014 Insufficient Information 1 Device
2014 Improper or Incorrect Procedure or Method 2 Device
2014 Device Tipped Over 1 Device
2014 Device Slipped 3 Device
2014 Device Inoperable 2 Device
2014 Connection Problem 1 Device
2014 Component Missing 1 Device
2014 Component Falling 2 Device
2014 Break 5 Device
2014 Bent 2 Device
2013 Scratched Material 1 Device
2013 Retraction Problem 1 Device
2013 Material Puncture/Hole 1 Device
2013 Device Operates Differently Than Expected 1 Device
2013 Detachment Of Device Component 1 Device
2013 Crack 2 Device
2013 Component Falling 1 Device
2013 Bent 1 Device