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TPLC
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show TPLC since
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
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Device
lipoprotein, low density, removal
Product Code
MMY
Device Class
3
Premarket Approvals (PMA)
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
3
2
0
3
1
0
5
7
3
3
4
2
3
3
1
1
MDR Year
MDR Reports
MDR Events
2014
6
6
2015
1
1
2016
5
5
2017
2
2
2018
4
4
2019
2
2
2020
2
2
2022
1
1
Device Problems
MDRs with this Device Problem
Events in those MDRs
Adverse Event Without Identified Device or Use Problem
14
14
Patient Device Interaction Problem
3
3
Use of Device Problem
2
2
Improper or Incorrect Procedure or Method
2
2
Break
1
1
Device Operates Differently Than Expected
1
1
Insufficient Information
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
Low Blood Pressure/ Hypotension
16
16
Loss of consciousness
7
7
Apheresis
6
6
Edema
4
4
Death
3
3
Anaphylactoid
2
2
Cardiopulmonary Arrest
2
2
Shock
2
2
Anaphylactic Shock
2
2
Hypovolemia
2
2
Hypovolemic Shock
1
1
Arrhythmia
1
1
Sweating
1
1
Hypersensitivity/Allergic reaction
1
1
Respiratory Distress
1
1
Heart Failure
1
1
Malaise
1
1
Cardiac Arrest
1
1
No Known Impact Or Consequence To Patient
1
1
Hemorrhage, Intraventricular
1
1
Disseminated Intravascular Coagulation (DIC)
1
1
Torsades-de-Pointes
1
1
Dyspnea
1
1
Tachycardia
1
1
Sudden Cardiac Death
1
1
Embolism
1
1
Hemorrhage/Bleeding
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Kaneka America Corp
II
Apr-09-2022
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