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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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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
ACCURATE MEDICAL THERAPEUTICS, LTD.
  SUBSTANTIALLY EQUIVALENT 2
BIOPTIMAL INTERNATIONAL PTE. , 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
SPECTRUM VASCULAR
  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 391 397
2024 511 511
2025 665 665
2026 364 364

Device Problems MDRs with this Device Problem Events in those MDRs
Material Separation 622 622
Fracture 611 611
Detachment of Device or Device Component 420 420
Difficult to Remove 230 230
Degraded 200 200
Break 197 199
Adverse Event Without Identified Device or Use Problem 195 201
Crack 147 147
Material Split, Cut or Torn 92 92
Difficult to Advance 82 82
Fluid/Blood Leak 74 74
Material Puncture/Hole 58 58
Device Contamination with Chemical or Other Material 56 56
Physical Resistance/Sticking 47 47
Leak/Splash 46 46
Material Deformation 44 44
Deformation Due to Compressive Stress 40 40
Failure to Advance 40 40
Entrapment of Device 38 38
Communication or Transmission Problem 35 35
Material Fragmentation 33 33
Device Contaminated During Manufacture or Shipping 33 33
Material Protrusion/Extrusion 33 33
No Display/Image 32 32
Material Integrity Problem 32 32
Stretched 31 31
Peeled/Delaminated 31 31
Mechanical Problem 28 28
Material Twisted/Bent 27 27
Tear, Rip or Hole in Device Packaging 26 26
Poor Quality Image 23 23
Difficult to Insert 21 21
Incorrect, Inadequate or Imprecise Result or Readings 21 21
Material Rupture 21 21
Improper or Incorrect Procedure or Method 20 20
Material Frayed 19 19
Difficult or Delayed Positioning 18 18
Device-Device Incompatibility 17 17
Gas/Air Leak 16 16
Defective Component 15 15
Unable to Obtain Readings 15 15
Obstruction of Flow 15 15
Defective Device 13 13
Contamination 13 13
Separation Problem 13 13
Disconnection 13 13
Use of Device Problem 13 13
Air/Gas in Device 12 12
Unraveled Material 11 11
Difficult to Open or Remove Packaging Material 10 10

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 2038 2039
Foreign Body In Patient 317 317
No Consequences Or Impact To Patient 115 115
Insufficient Information 102 103
Vascular Dissection 90 90
No Known Impact Or Consequence To Patient 39 39
No Patient Involvement 38 38
Thrombosis/Thrombus 34 34
Device Embedded In Tissue or Plaque 30 30
Obstruction/Occlusion 27 30
Stroke/CVA 24 26
No Code Available 20 20
Perforation of Vessels 18 18
Vasoconstriction 16 16
Cardiac Arrest 16 16
Hemorrhage/Blood Loss/Bleeding 16 16
Non specific EKG/ECG Changes 14 14
Chest Pain 14 14
Air Embolism 13 13
Low Blood Pressure/ Hypotension 13 13
Pericardial Effusion 12 12
Intracranial Hemorrhage 11 11
Ischemia 10 10
Cardiac Tamponade 10 10
Ischemia Stroke 10 10
Ventricular Fibrillation 9 9
Rupture 8 8
Cardiac Perforation 8 8
Pain 8 8
Speech Disorder 8 8
Facial Paralysis 7 7
Myocardial Infarction 7 7
Hematoma 7 7
Angina 6 6
Death 6 6
Dyspnea 6 6
Muscle Weakness/Atrophy 6 6
Diplopia/Double Vision 6 6
Embolism/Embolus 5 5
Occlusion 5 5
Paralysis 5 5
Cardiogenic Shock 5 5
Arrhythmia 5 5
Bradycardia 5 5
Failure of Implant 5 5
Hypersensitivity/Allergic reaction 4 4
Infiltration into Tissue 4 4
Paresis 4 5
Renal Failure 4 4
Thromboembolism 4 5

Recalls
Manufacturer Recall Class Date Posted
1 Abbott Vascular I May-19-2022
2 Angiodynamics, Inc. II Apr-17-2026
3 Angiodynamics, Inc. II Jul-31-2024
4 Boston Scientific Corporation I May-10-2024
5 Boston Scientific Corporation I Mar-25-2020
6 Cook Incorporated I May-01-2026
7 Cook Incorporated II Apr-06-2026
8 Cook Incorporated I Jun-16-2025
9 Cordis Corporation I Sep-15-2021
10 Cordis US Corp I Nov-09-2023
11 Cordis US Corp II Dec-16-2022
12 Gentuity, LLC II Apr-16-2026
13 Stryker Neurovascular II May-28-2024
14 Stryker Neurovascular II Jul-15-2022
15 Stryker, Inc. II Feb-14-2024
16 Vascular Solutions, Inc. I Oct-20-2020
17 Vascular Solutions, Inc. I Apr-27-2020
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