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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Super Search Devices@FDA
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New Search show TPLC since Back to Search Results
Device catheter, intravascular, diagnostic
Regulation Description Diagnostic intravascular catheter.
Product CodeDQO
Regulation Number 870.1200
Device Class 2


Premarket Reviews
ManufacturerDecision
ABBOTT MEDICAL
  SUBSTANTIALLY EQUIVALENT 1
ACCURATE MEDICAL THERAPEUTICS
  SUBSTANTIALLY EQUIVALENT 1
  1.  K203487  Drakon and Sequre Microcatheters
ACCURATE MEDICAL THERAPEUTICS LTD
  SUBSTANTIALLY EQUIVALENT 1
  1.  K203487  Drakon and Sequre Microcatheters
ACCURATE MEDICAL THERAPEUTICS LTD.
  SUBSTANTIALLY EQUIVALENT 1
CORDIS CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
CORDIS US CORP.
  SUBSTANTIALLY EQUIVALENT 1
EMBOLX, INC.
  SUBSTANTIALLY EQUIVALENT 1
GENTUITY, LLC
  SUBSTANTIALLY EQUIVALENT 2
IMPERATIVE CARE, INC.
  SUBSTANTIALLY EQUIVALENT 1
MERIT MEDICAL SYSTEMS, INC.
  SUBSTANTIALLY EQUIVALENT 1
PFM MEDICAL, INC.
  SUBSTANTIALLY EQUIVALENT 1
PHENOX LTD
  SUBSTANTIALLY EQUIVALENT 2
SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
SUZHOU HENGRUI DISHENG MEDICAL CO.,LTD.
  SUBSTANTIALLY EQUIVALENT 1
TERUMO CLINICAL SUPPLY CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
TERUMO CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
VASCULAR SOLUTIONS LLC
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2020 312 312
2021 338 340
2022 379 379
2023 391 391
2024 511 511
2025 530 530

Device Problems MDRs with this Device Problem Events in those MDRs
Material Separation 587 587
Fracture 567 567
Detachment of Device or Device Component 302 302
Difficult to Remove 199 199
Adverse Event Without Identified Device or Use Problem 178 178
Break 159 161
Crack 112 112
Degraded 110 110
Difficult to Advance 74 74
Material Split, Cut or Torn 73 73
Fluid/Blood Leak 65 65
Material Puncture/Hole 53 53
Device Contamination with Chemical or Other Material 49 49
Physical Resistance/Sticking 42 42
Material Deformation 41 41
Leak/Splash 37 37
Failure to Advance 36 36
Entrapment of Device 35 35
Deformation Due to Compressive Stress 33 33
Device Contaminated During Manufacture or Shipping 33 33
Communication or Transmission Problem 28 28
Material Integrity Problem 27 27
Material Twisted/Bent 26 26
Tear, Rip or Hole in Device Packaging 25 25
Peeled/Delaminated 24 24
Material Protrusion/Extrusion 24 24
Stretched 24 24
No Display/Image 22 22
Material Fragmentation 22 22
Material Rupture 20 20
Difficult to Insert 20 20
Incorrect, Inadequate or Imprecise Result or Readings 20 20
Poor Quality Image 19 19
Material Frayed 18 18
Difficult or Delayed Positioning 17 17
Gas/Air Leak 16 16
Device-Device Incompatibility 16 16
Improper or Incorrect Procedure or Method 16 16
Unable to Obtain Readings 15 15
Defective Component 15 15
Separation Problem 13 13
Obstruction of Flow 13 13
Use of Device Problem 12 12
Disconnection 12 12
Contamination 11 11
Defective Device 10 10
Burst Container or Vessel 10 10
Difficult to Open or Remove Packaging Material 10 10
Contamination /Decontamination Problem 9 9
Unraveled Material 9 9

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 1624 1625
Foreign Body In Patient 271 271
No Consequences Or Impact To Patient 115 115
Insufficient Information 82 83
Vascular Dissection 82 82
No Known Impact Or Consequence To Patient 39 39
No Patient Involvement 38 38
Thrombosis/Thrombus 33 33
Device Embedded In Tissue or Plaque 29 29
Obstruction/Occlusion 26 26
Stroke/CVA 23 23
No Code Available 20 20
Perforation of Vessels 18 18
Cardiac Arrest 16 16
Vasoconstriction 15 15
Hemorrhage/Bleeding 14 14
Chest Pain 14 14
Non specific EKG/ECG Changes 13 13
Air Embolism 11 11
Intracranial Hemorrhage 11 11
Low Blood Pressure/ Hypotension 10 10
Ischemia 10 10
Pericardial Effusion 10 10
Ventricular Fibrillation 9 9
Speech Disorder 8 8
Pain 8 8
Rupture 8 8
Cardiac Perforation 7 7
Hematoma 7 7
Ischemia Stroke 6 6
Myocardial Infarction 6 6
Death 6 6
Dyspnea 6 6
Muscle Weakness 6 6
Bradycardia 5 5
Cardiogenic Shock 5 5
Paralysis 5 5
Angina 5 5
Cardiac Tamponade 5 5
Arrhythmia 5 5
Embolism/Embolus 5 5
Occlusion 5 5
Failure of Implant 5 5
Infiltration into Tissue 4 4
Pseudoaneurysm 4 4
Hypersensitivity/Allergic reaction 4 4
Renal Failure 4 4
Thromboembolism 4 4
Paresis 4 4
Encephalopathy 3 3

Recalls
Manufacturer Recall Class Date Posted
1 Abbott Vascular I May-19-2022
2 Angiodynamics, Inc. II Jul-31-2024
3 Boston Scientific Corporation I May-10-2024
4 Boston Scientific Corporation I Mar-25-2020
5 Cook Incorporated I Jun-16-2025
6 Cordis Corporation I Sep-15-2021
7 Cordis US Corp I Nov-09-2023
8 Cordis US Corp II Dec-16-2022
9 Stryker Neurovascular II May-28-2024
10 Stryker Neurovascular II Jul-15-2022
11 Stryker, Inc. II Feb-14-2024
12 Vascular Solutions, Inc. I Oct-20-2020
13 Vascular Solutions, Inc. I Apr-27-2020
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