MAGIC 3 CATHETER
This device is manufactured by CR BARD (COVINGTON) -1018233.
The following problems were reported about this device:
Year | Description | Events/year | Type |
---|---|---|---|
2024 | Urinary Tract Infection | 2 | Patient |
2024 | Skin Inflammation/ Irritation | 2 | Patient |
2024 | Discomfort | 2 | Patient |
2024 | Appropriate Term / Code Not Available | 3 | Patient |
2024 | Abrasion | 1 | Patient |
2024 | Sharp Edges | 1 | Device |
2024 | Partial Blockage | 1 | Device |
2024 | Incorrect Measurement | 1 | Device |
2024 | Inaccurate Flow Rate | 1 | Device |
2024 | Improper Chemical Reaction | 6 | Device |
2024 | Difficult to Insert | 1 | Device |
2024 | Component Misassembled | 3 | Device |
2024 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
2023 | Urinary Tract Infection | 2 | Patient |
2023 | Pain | 1 | Patient |
2023 | Discomfort | 1 | Patient |
2023 | Appropriate Term / Code Not Available | 2 | Patient |
2023 | Short Fill | 1 | Device |
2023 | Material Twisted/Bent | 2 | Device |
2023 | Material Protrusion/Extrusion | 1 | Device |
2023 | Incomplete or Missing Packaging | 1 | Device |
2023 | Improper Chemical Reaction | 7 | Device |
2023 | Difficult to Insert | 2 | Device |
2023 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
2022 | Short Fill | 4 | Device |
2022 | Sharp Edges | 1 | Device |
2022 | Material Fragmentation | 1 | Device |
2022 | Incorrect Measurement | 1 | Device |
2022 | Inaccurate Flow Rate | 1 | Device |
2022 | Difficult to Insert | 2 | Device |
2022 | Component Misassembled | 1 | Device |
2021 | Inadequacy of Device Shape and/or Size | 1 | Device |
2021 | Adverse Event Without Identified Device or Use Problem | 1 | Device |
2019 | Unsealed Device Packaging | 1 | Device |
2019 | Therapeutic or Diagnostic Output Failure | 8 | Device |
2019 | Tear, Rip or Hole in Device Packaging | 3 | Device |
2019 | Structural Problem | 2 | Device |
2019 | Short Fill | 20 | Device |
2019 | Sharp Edges | 1 | Device |
2019 | Scratched Material | 7 | Device |
2019 | Product Quality Problem | 60 | Device |
2019 | Physical Resistance/Sticking | 5 | Device |
2019 | Patient-Device Incompatibility | 12 | Device |
2019 | Packaging Problem | 1 | Device |
2019 | Output Problem | 1 | Device |
2019 | Obstruction of Flow | 1 | Device |
2019 | Nonstandard Device | 4 | Device |
2019 | No Flow | 2 | Device |
2019 | Moisture or Humidity Problem | 3 | Device |
2019 | Misassembled | 10 | Device |
2019 | Material Twisted/Bent | 17 | Device |
2019 | Material Too Rigid or Stiff | 2 | Device |
2019 | Material Split, Cut or Torn | 2 | Device |
2019 | Material Rupture | 1 | Device |
2019 | Material Puncture/Hole | 2 | Device |
2019 | Material Integrity Problem | 26 | Device |
2019 | Material Discolored | 1 | Device |
2019 | Material Deformation | 4 | Device |
2019 | Manufacturing, Packaging or Shipping Problem | 2 | Device |
2019 | Insufficient Information | 2 | Device |
2019 | Incorrect Measurement | 23 | Device |
2019 | Inadequacy of Device Shape and/or Size | 9 | Device |
2019 | Inaccurate Flow Rate | 2 | Device |
2019 | Improper or Incorrect Procedure or Method | 1 | Device |
2019 | Gel Leak | 4 | Device |
2019 | Gas/Air Leak | 1 | Device |
2019 | Difficult to Remove | 1 | Device |
2019 | Difficult to Insert | 45 | Device |
2019 | Device Damaged Prior to Use | 19 | Device |
2019 | Device Contamination with Chemical or Other Material | 2 | Device |
2019 | Deformation Due to Compressive Stress | 1 | Device |
2019 | Defective Device | 3 | Device |
2019 | Component Missing | 18 | Device |
2019 | Burst Container or Vessel | 5 | Device |
2019 | Break | 7 | Device |
2019 | Appropriate Term/Code Not Available | 2 | Device |
2019 | Adverse Event Without Identified Device or Use Problem | 6 | Device |
2018 | Use of Device Problem | 2 | Device |
2018 | Unstable | 1 | Device |
2018 | Unsealed Device Packaging | 2 | Device |
2018 | Tear, Rip or Hole in Device Packaging | 8 | Device |
2018 | Structural Problem | 1 | Device |
2018 | Sticking | 2 | Device |
2018 | Split | 1 | Device |
2018 | Short Fill | 38 | Device |
2018 | Sharp Edges | 1 | Device |
2018 | Scratched Material | 3 | Device |
2018 | Restricted Flow rate | 1 | Device |
2018 | Protective Measures Problem | 2 | Device |
2018 | Product Quality Problem | 90 | Device |
2018 | Problem with Sterilization | 1 | Device |
2018 | Positioning Problem | 2 | Device |
2018 | Physical Resistance/Sticking | 4 | Device |
2018 | Physical Resistance | 1 | Device |
2018 | Physical Property Issue | 2 | Device |
2018 | Patient-Device Incompatibility | 29 | Device |
2018 | Partial Blockage | 1 | Device |
2018 | Packaging Problem | 1 | Device |
2018 | Overfill | 1 | Device |
2018 | Out-Of-Box Failure | 3 | Device |
2018 | Obstruction of Flow | 3 | Device |
2018 | Nonstandard Device | 6 | Device |
2018 | No Flow | 10 | Device |
2018 | Moisture or Humidity Problem | 7 | Device |
2018 | Misassembled | 14 | Device |
2018 | Mechanics Altered | 1 | Device |
2018 | Mechanical Problem | 1 | Device |
2018 | Material Twisted/Bent | 18 | Device |
2018 | Material Split, Cut or Torn | 4 | Device |
2018 | Material Rupture | 1 | Device |
2018 | Material Puncture/Hole | 3 | Device |
2018 | Material Protrusion/Extrusion | 2 | Device |
2018 | Material Integrity Problem | 58 | Device |
2018 | Material Deformation | 6 | Device |
2018 | Manufacturing, Packaging or Shipping Problem | 7 | Device |
2018 | Leak/Splash | 3 | Device |
2018 | Insufficient Information | 5 | Device |
2018 | Infusion or Flow Problem | 1 | Device |
2018 | Incorrect Measurement | 30 | Device |
2018 | Incomplete or Missing Packaging | 1 | Device |
2018 | Inadequate Instructions for Healthcare Professional | 1 | Device |
2018 | Inadequacy of Device Shape and/or Size | 10 | Device |
2018 | Inaccurate Flow Rate | 12 | Device |
2018 | Improper or Incorrect Procedure or Method | 1 | Device |
2018 | Improper Flow or Infusion | 1 | Device |
2018 | Hole In Material | 1 | Device |
2018 | Gel Leak | 1 | Device |
2018 | Gas/Air Leak | 1 | Device |
2018 | Fluid/Blood Leak | 6 | Device |
2018 | Filling Problem | 4 | Device |
2018 | Failure to Cut | 1 | Device |
2018 | Failure to Advance | 2 | Device |
2018 | Difficult to Remove | 3 | Device |
2018 | Difficult to Insert | 41 | Device |
2018 | Difficult to Advance | 1 | Device |
2018 | Device Operational Issue | 1 | Device |
2018 | Device Operates Differently Than Expected | 23 | Device |
2018 | Device Damaged Prior to Use | 20 | Device |
2018 | Device Contamination with Chemical or Other Material | 1 | Device |
2018 | Detachment of Device or Device Component | 1 | Device |
2018 | Defective Device | 2 | Device |
2018 | Cut In Material | 1 | Device |
2018 | Crack | 1 | Device |
2018 | Contamination | 1 | Device |
2018 | Component Missing | 41 | Device |
2018 | Component Incompatible | 1 | Device |
2018 | Compatibility Problem | 3 | Device |
2018 | Burst Container or Vessel | 6 | Device |
2018 | Break | 4 | Device |
2018 | Bent | 8 | Device |
2018 | Appropriate Term/Code Not Available | 9 | Device |
2018 | Adverse Event Without Identified Device or Use Problem | 18 | Device |
2018 | Activation Problem | 1 | Device |
2017 | Use of Device Problem | 1 | Device |
2017 | Unsealed Device Packaging | 2 | Device |
2017 | Tear, Rip or Hole in Device Packaging | 1 | Device |
2017 | Sticking | 1 | Device |
2017 | Split | 1 | Device |
2017 | Short Fill | 4 | Device |
2017 | Scratched Material | 5 | Device |
2017 | Product Quality Problem | 27 | Device |
2017 | Physical Resistance | 2 | Device |
2017 | Patient-Device Incompatibility | 8 | Device |
2017 | Packaging Problem | 2 | Device |
2017 | Out-Of-Box Failure | 3 | Device |
2017 | Nonstandard Device | 18 | Device |
2017 | No Flow | 2 | Device |
2017 | Moisture or Humidity Problem | 1 | Device |
2017 | Mechanical Problem | 2 | Device |
2017 | Material Puncture/Hole | 1 | Device |
2017 | Material Integrity Problem | 14 | Device |
2017 | Material Deformation | 6 | Device |
2017 | Insufficient Information | 6 | Device |
2017 | Improper or Incorrect Procedure or Method | 4 | Device |
2017 | Fluid/Blood Leak | 5 | Device |
2017 | Filling Problem | 2 | Device |
2017 | Failure to Advance | 5 | Device |
2017 | Difficult to Remove | 2 | Device |
2017 | Difficult to Insert | 15 | Device |
2017 | Difficult to Advance | 1 | Device |
2017 | Device Operates Differently Than Expected | 21 | Device |
2017 | Device Inoperable | 1 | Device |
2017 | Device Damaged Prior to Use | 1 | Device |
2017 | Delivered as Unsterile Product | 1 | Device |
2017 | Defective Device | 1 | Device |
2017 | Defective Component | 3 | Device |
2017 | Cut In Material | 5 | Device |
2017 | Component Missing | 25 | Device |
2017 | Complete Blockage | 1 | Device |
2017 | Clumping in Device or Device Ingredient | 1 | Device |
2017 | Burst Container or Vessel | 2 | Device |
2017 | Bent | 5 | Device |
2017 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
2016 | Patient-Device Incompatibility | 1 | Device |