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TPLC
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show TPLC since
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2024
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Device
cannula, catheter
Product Code
DQR
Regulation Number
870.1300
Device Class
2
MDR Year
MDR Reports
MDR Events
2019
16
16
2020
4
4
2021
11
11
2022
27
27
2023
36
36
2024
8
8
Device Problems
MDRs with this Device Problem
Events in those MDRs
Break
21
21
Fluid/Blood Leak
20
20
Insufficient Information
14
14
Adverse Event Without Identified Device or Use Problem
12
12
Detachment of Device or Device Component
8
8
Leak/Splash
4
4
Fail-Safe Problem
3
3
Material Deformation
3
3
Material Puncture/Hole
3
3
Air/Gas in Device
3
3
Device Displays Incorrect Message
2
2
Fracture
2
2
Crack
2
2
Labelling, Instructions for Use or Training Problem
2
2
Failure to Advance
1
1
Disconnection
1
1
Gas/Air Leak
1
1
Material Split, Cut or Torn
1
1
Reflux within Device
1
1
Loose or Intermittent Connection
1
1
Protective Measures Problem
1
1
Separation Problem
1
1
Defective Component
1
1
No Flow
1
1
Material Twisted/Bent
1
1
Output Problem
1
1
Device Contaminated During Manufacture or Shipping
1
1
Material Separation
1
1
Tear, Rip or Hole in Device Packaging
1
1
Material Fragmentation
1
1
Difficult to Remove
1
1
Complete Blockage
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
34
34
Hemorrhage/Bleeding
20
20
Foreign Body In Patient
14
14
Insufficient Information
7
7
No Known Impact Or Consequence To Patient
7
7
Device Embedded In Tissue or Plaque
5
5
No Consequences Or Impact To Patient
3
3
Needle Stick/Puncture
3
3
Hematoma
2
2
Encephalopathy
1
1
Obstruction/Occlusion
1
1
Embolus
1
1
Neurological Deficit/Dysfunction
1
1
Hematuria
1
1
Hypoxia
1
1
Blood Loss
1
1
Low Blood Pressure/ Hypotension
1
1
Ventilator Dependent
1
1
Thromboembolism
1
1
Exposure to Body Fluids
1
1
No Information
1
1
Cardiac Arrest
1
1
Death
1
1
Discomfort
1
1
Dysphasia
1
1
Headache
1
1
No Patient Involvement
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Angiodynamics, Inc.
II
Nov-05-2020
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