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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
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Device stent, iliac vein
Definition A metal scaffold placed via a delivery catheter in the iliac vein to maintain the lumen
Product CodeQAN
Device Class 3

Premarket Approvals (PMA)
2019 2020 2021 2022 2023 2024
4 10 11 5 7 7

MDR Year MDR Reports MDR Events
2019 24 24
2020 117 117
2021 425 425
2022 115 115
2023 208 208
2024 82 82

Device Problems MDRs with this Device Problem Events in those MDRs
Activation Failure 417 417
Adverse Event Without Identified Device or Use Problem 128 128
Material Deformation 84 84
Migration 83 83
Activation, Positioning or Separation Problem 58 58
Fracture 58 58
Improper or Incorrect Procedure or Method 44 44
Migration or Expulsion of Device 37 37
Off-Label Use 34 34
Positioning Failure 33 33
Entrapment of Device 30 30
Use of Device Problem 26 26
Difficult to Remove 26 26
Misfire 25 25
Malposition of Device 23 23
Break 21 21
Difficult or Delayed Positioning 20 20
Deformation Due to Compressive Stress 18 18
Detachment of Device or Device Component 17 17
Premature Activation 12 12
Obstruction of Flow 11 11
Material Twisted/Bent 10 10
Positioning Problem 9 9
No Apparent Adverse Event 8 8
Difficult to Advance 8 8
Device Damaged by Another Device 7 7
Physical Resistance/Sticking 7 7
Device-Device Incompatibility 7 7
Structural Problem 6 6
Device Markings/Labelling Problem 6 6
Loss of or Failure to Bond 5 5
Material Fragmentation 4 4
Appropriate Term/Code Not Available 4 4
Failure to Advance 4 4
Activation Problem 4 4
Mechanical Problem 4 4
Nonstandard Device 3 3
Material Integrity Problem 3 3
Defective Device 3 3
Device Damaged Prior to Use 3 3
Device Dislodged or Dislocated 2 2
Human-Device Interface Problem 2 2
Inaccurate Information 2 2
Biocompatibility 2 2
Material Separation 2 2
Retraction Problem 2 2
Delivered as Unsterile Product 2 2
Difficult or Delayed Activation 2 2
Material Too Rigid or Stiff 2 2
Stretched 2 2

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 665 665
Thrombosis/Thrombus 73 73
Obstruction/Occlusion 46 46
Insufficient Information 44 44
Pain 31 31
No Consequences Or Impact To Patient 27 27
Restenosis 25 25
Chest Pain 15 15
Stenosis 14 14
Swelling/ Edema 13 13
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 12 12
Dyspnea 12 12
Device Embedded In Tissue or Plaque 9 9
No Known Impact Or Consequence To Patient 8 8
Unspecified Tissue Injury 7 7
Hypersensitivity/Allergic reaction 6 6
Perforation 6 6
Foreign Body In Patient 6 6
Pulmonary Embolism 5 5
Failure of Implant 5 5
No Code Available 5 5
Swelling 5 5
Injury 5 5
Unintended Radiation Exposure 4 4
Hemorrhage/Bleeding 4 4
Unspecified Heart Problem 4 4
Reocclusion 4 4
Thrombosis 4 4
Stroke/CVA 4 4
Cellulitis 3 3
Tachycardia 3 3
Arrhythmia 3 3
Stacking Breaths 3 3
Fever 2 2
Paralysis 2 2
Pericardial Effusion 2 2
Local Reaction 2 2
Atrial Fibrillation 2 2
Nerve Damage 2 2
No Patient Involvement 2 2
Foreign Body Embolism 2 2
Embolism/Embolus 2 2
Occlusion 2 2
Pancreatitis 2 2
Ulcer 2 2
Respiratory Insufficiency 2 2
Rupture 1 1
Edema 1 1
Cardiac Tamponade 1 1
Rash 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Bard Peripheral Vascular Inc II Jun-17-2021
2 Boston Scientific Corporation I May-19-2021
3 Medtronic Inc. II Mar-19-2024
4 Medtronic Inc. II May-05-2021
5 Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) II Jan-06-2022
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