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Device
trocar
Regulation Description
Trocar.
Product Code
DRC
Regulation Number
870.1390
Device Class
2
Premarket Reviews
Manufacturer
Decision
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
Gas/Air Leak
11
11
Insufficient Device Problem Information
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
No Apparent Adverse Event
4
4
Material Puncture/Hole
4
4
Difficult to Advance
4
4
Detachment of Device or Device Component
4
4
Positioning Problem
3
3
Patient Device Interaction Problem
3
3
Physical Resistance/Sticking
3
3
Corroded
3
3
Device Contaminated During Manufacture or Shipping
2
2
Difficult to Remove
2
2
Device Contamination with Chemical or Other Material
2
2
Fluid/Blood Leak
2
2
Obstruction of Flow
2
2
Material Protrusion/Extrusion
1
1
Compatibility Problem
1
1
Noise, Audible
1
1
Unsealed Device Packaging
1
1
Off-Label Use
1
1
Inadequacy of Device Shape and/or Size
1
1
Contamination
1
1
Positioning Failure
1
1
Device-Device Incompatibility
1
1
Material Fragmentation
1
1
Contamination /Decontamination Problem
1
1
Component Missing
1
1
Patient-Device Incompatibility
1
1
Dull, Blunt
1
1
Structural Problem
1
1
Failure to Disconnect
1
1
Malposition of Device
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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