MAGIC3 INTERMITTENT CATHETER WITH SURE-GRIP SLEEVE

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