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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device trocar
Regulation Description Trocar.
Product CodeDRC
Regulation Number 870.1390
Device Class 2


Premarket Reviews
ManufacturerDecision
PRESSURE PRODUCTS MEDICAL DEVICE MANUFACTURING, LLC
  SUBSTANTIALLY EQUIVALENT 3
SHANGHAI MICROPORT EP MEDTECH CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
SYNAPTIC MEDICAL CORPORATION
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2021 78 78
2022 61 63
2023 109 109
2024 105 107
2025 70 70
2026 53 53

Device Problems MDRs with this Device Problem Events in those MDRs
Adverse Event Without Identified Device or Use Problem 292 296
Difficult to Insert 26 27
Fracture 25 25
Break 15 15
Insufficient Device Problem Information 11 11
Gas/Air Leak 11 11
Unintended Movement 9 9
Material Twisted/Bent 9 9
Material Separation 8 8
Improper or Incorrect Procedure or Method 7 7
Device Contamination with Body Fluid 6 6
Material Puncture/Hole 4 4
No Apparent Adverse Event 4 4
Difficult to Advance 4 4
Detachment of Device or Device Component 4 4
Physical Resistance/Sticking 3 3
Patient Device Interaction Problem 3 3
Positioning Problem 3 3
Corroded 3 3
Device Contamination with Chemical or Other Material 2 2
Device Contaminated During Manufacture or Shipping 2 2
Fluid/Blood Leak 2 2
Obstruction of Flow 2 2
Difficult to Remove 2 2
Contamination /Decontamination Problem 1 1
Device-Device Incompatibility 1 1
Patient-Device Incompatibility 1 1
Material Fragmentation 1 1
Compatibility Problem 1 1
Material Protrusion/Extrusion 1 1
Positioning Failure 1 1
Contamination 1 1
Malposition of Device 1 1
Failure to Disconnect 1 1
Noise, Audible 1 1
Structural Problem 1 1
Unsealed Device Packaging 1 1
Off-Label Use 1 1
Dull, Blunt 1 1
Component Missing 1 1
Inadequacy of Device Shape and/or Size 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
Cardiac Perforation 232 236
No Clinical Signs, Symptoms or Conditions 117 117
Pericardial Effusion 51 51
Cardiac Tamponade 37 37
Low Blood Pressure/ Hypotension 27 27
Great Vessel Perforation 13 13
Thrombosis/Thrombus 10 10
Perforation 9 9
Hemorrhage/Blood Loss/Bleeding 8 8
Arrhythmia 7 7
Insufficient Information 7 7
Stroke/CVA 5 5
Foreign Body In Patient 5 5
Hematoma 4 4
Asystole 4 4
Cardiac Arrest 4 4
Pseudoaneurysm 4 4
Needle Stick/Puncture 4 4
Vascular Dissection 2 2
Transient Ischemic Attack 2 2
Bradycardia 2 2
Air Embolism 2 2
Non specific EKG/ECG Changes 2 2
Fistula 2 2
Unspecified Tissue Injury 2 2
Perforation of Vessels 2 2
Hypoxia 1 1
Embolism/Embolus 1 1
Cognitive Changes 1 1
Scar Tissue 1 1
Low Oxygen Saturation 1 1
Respiratory Arrest 1 1
Ventricular Fibrillation 1 1
No Consequences Or Impact To Patient 1 1
Myocardial Infarction 1 1
Superficial (First Degree) Burn 1 1
Unspecified Mental, Emotional or Behavioural Problem 1 1
Foreign Body Embolism 1 1
Hypersensitivity/Allergic reaction 1 1
Heart Failure/Congestive Heart Failure 1 1
Dizziness 1 1
Unspecified Vascular Problem 1 1
Discomfort 1 1
Device Embedded In Tissue or Plaque 1 1
Diplopia/Double Vision 1 1
Chest Pain 1 1
Atrial Fibrillation 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Cook Inc. II Nov-13-2021
2 Cook Incorporated II Apr-12-2024
3 Merit Medical Systems, Inc. II Mar-16-2021
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