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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
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Device catheter, flow directed
Product CodeDYG
Regulation Number 870.1240
Device Class 2


Premarket Reviews
ManufacturerDecision
EDWARDS LIFESCIENCES, LLC
  SUBSTANTIALLY EQUIVALENT 1
EDWARDS LIFESCIENCESS LLC
  SUBSTANTIALLY EQUIVALENT 1
EDWARDS LIFESIENCES, LLC
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2017 115 115
2018 133 133
2019 144 144
2020 104 104
2021 97 97
2022 130 130
2023 227 227
2024 66 66

Device Problems MDRs with this Device Problem Events in those MDRs
Material Rupture 137 137
Pacing Problem 93 93
Incorrect Measurement 88 88
Inflation Problem 87 87
Incorrect, Inadequate or Imprecise Result or Readings 84 84
Deflation Problem 76 76
Adverse Event Without Identified Device or Use Problem 54 54
Leak/Splash 47 47
Appropriate Term/Code Not Available 38 38
Difficult to Advance 33 33
Failure to Capture 33 33
Material Separation 28 28
Burst Container or Vessel 25 25
Break 24 24
Detachment of Device or Device Component 22 22
Material Split, Cut or Torn 22 22
Physical Resistance/Sticking 22 22
Fluid/Blood Leak 16 16
Difficult to Remove 16 16
No Pacing 15 15
Material Deformation 12 12
Material Puncture/Hole 12 12
No Device Output 11 11
Failure to Deflate 11 11
Difficult to Insert 10 10
Component Missing 9 9
Defective Device 9 9
Material Integrity Problem 8 8
Unable to Obtain Readings 8 8
Difficult or Delayed Positioning 8 8
Material Fragmentation 7 7
Entrapment of Device 6 6
Detachment Of Device Component 6 6
Obstruction of Flow 6 6
Output Problem 6 6
Activation, Positioning or Separation Problem 6 6
Material Twisted/Bent 6 6
Insufficient Information 5 5
Failure to Advance 5 5
Defective Component 5 5
Use of Device Problem 4 4
Insufficient Flow or Under Infusion 4 4
Connection Problem 4 4
Patient-Device Incompatibility 4 4
Temperature Problem 4 4
Therapeutic or Diagnostic Output Failure 4 4
Gas/Air Leak 4 4
Activation Failure 4 4
Inaccurate Information 4 4
Device Contamination with Chemical or Other Material 3 3
Unintended Movement 3 3
Device Displays Incorrect Message 3 3
Malposition of Device 3 3
Failure to Calibrate 3 3
High Test Results 3 3
Product Quality Problem 3 3
Contamination 3 3
Crack 3 3
Flaked 3 3
Difficult to Flush 3 3
Mechanical Problem 3 3
Disconnection 2 2
Complete Blockage 2 2
Air Leak 2 2
Device Alarm System 2 2
Signal Artifact/Noise 2 2
Pacing Inadequately 2 2
Tear, Rip or Hole in Device Packaging 2 2
High Readings 2 2
Capturing Problem 2 2
Device Operates Differently Than Expected 2 2
Device Dislodged or Dislocated 2 2
Material Protrusion/Extrusion 2 2
Separation Problem 2 2
Data Problem 2 2
Device Handling Problem 1 1
Unclear Information 1 1
Unintended Deflation 1 1
Device Contaminated During Manufacture or Shipping 1 1
No Apparent Adverse Event 1 1
Packaging Problem 1 1
Pressure Problem 1 1
Protective Measures Problem 1 1
Contamination /Decontamination Problem 1 1
Communication or Transmission Problem 1 1
Deformation Due to Compressive Stress 1 1
Calibration Problem 1 1
Device Ingredient or Reagent Problem 1 1
Device Markings/Labelling Problem 1 1
Low Readings 1 1
Structural Problem 1 1
Difficult or Delayed Activation 1 1
Device Or Device Fragments Location Unknown 1 1
Device Contamination with Body Fluid 1 1
Inaccurate Delivery 1 1
Low Test Results 1 1
Device Damaged Prior to Use 1 1
Improper or Incorrect Procedure or Method 1 1
Shipping Damage or Problem 1 1
Inadequacy of Device Shape and/or Size 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 414 414
No Consequences Or Impact To Patient 314 314
No Known Impact Or Consequence To Patient 165 165
Insufficient Information 55 55
No Patient Involvement 23 23
Vascular Dissection 15 15
Hemorrhage/Bleeding 14 14
No Code Available 13 13
Arrhythmia 11 11
Cardiac Tamponade 10 10
No Information 9 9
Foreign Body In Patient 8 8
Low Blood Pressure/ Hypotension 8 8
Death 7 7
Cardiac Perforation 7 7
Device Embedded In Tissue or Plaque 7 7
Great Vessel Perforation 7 7
Cardiac Arrest 6 6
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 6 6
Bradycardia 5 5
Hypersensitivity/Allergic reaction 4 4
Pain 4 4
Needle Stick/Puncture 4 4
Complaint, Ill-Defined 3 3
Perforation of Vessels 3 3
Pericardial Effusion 3 3
High Blood Pressure/ Hypertension 3 3
Dyspnea 3 3
Chest Pain 3 3
Aortic Valve Stenosis 3 3
Atrial Fibrillation 3 3
Anaphylactic Shock 3 3
Pulmonary Embolism 2 2
Edema 2 2
Extravasation 2 2
Hemoptysis 2 2
Failure of Implant 2 2
Unspecified Infection 2 2
Myocardial Infarction 2 2
Perforation 2 2
Unspecified Vascular Problem 2 2
Low Oxygen Saturation 2 2
Dyskinesia 2 2
Reaction 2 2
Tingling 2 2
Rupture 2 2
Anaphylactoid 2 2
Renal Failure 2 2
Swelling/ Edema 2 2
Sepsis 1 1
Septic Shock 1 1
Shock 1 1
Therapeutic Effects, Unexpected 1 1
Thrombus 1 1
Tissue Damage 1 1
Loss of consciousness 1 1
Injury 1 1
Physical Entrapment 1 1
Ectopic Heartbeat 1 1
Vascular System (Circulation), Impaired 1 1
Blood Loss 1 1
Pseudoaneurysm 1 1
Complete Heart Block 1 1
Valvular Stenosis 1 1
Pneumothorax 1 1
Paresis 1 1
Necrosis 1 1
Left Ventricular Dysfunction 1 1
Non specific EKG/ECG Changes 1 1
Fever 1 1
Foreign Body Reaction 1 1
Headache 1 1
Cardiopulmonary Arrest 1 1
Air Embolism 1 1
Anemia 1 1
Aneurysm 1 1
Atrial Flutter 1 1
Autoimmune Reaction 1 1
Exposure to Body Fluids 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Arrow International Inc II Dec-19-2019
2 Edwards Lifesciences, LLC II Apr-12-2023
3 Edwards Lifesciences, LLC I Jan-31-2019
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