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TPLC
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Device
catheter, oximeter, fiber-optic
Product Code
DQE
Regulation Number
870.1230
Device Class
2
MDR Year
MDR Reports
MDR Events
2019
63
63
2020
39
39
2021
39
39
2022
57
57
2023
48
48
2024
47
47
Device Problems
MDRs with this Device Problem
Events in those MDRs
Incorrect, Inadequate or Imprecise Result or Readings
80
80
Material Rupture
55
55
Incorrect Measurement
29
29
Fluid/Blood Leak
22
22
Adverse Event Without Identified Device or Use Problem
16
16
Leak/Splash
13
13
Material Split, Cut or Torn
11
11
Deflation Problem
9
9
Appropriate Term/Code Not Available
9
9
Material Separation
8
8
Material Fragmentation
8
8
Unable to Obtain Readings
7
7
Inflation Problem
6
6
Break
6
6
Difficult to Insert
5
5
No Device Output
5
5
Detachment of Device or Device Component
5
5
Physical Resistance/Sticking
4
4
Output Problem
3
3
Insufficient Information
2
2
Defective Device
2
2
Display or Visual Feedback Problem
2
2
Device Displays Incorrect Message
2
2
Difficult to Remove
2
2
Microbial Contamination of Device
2
2
Increase in Pressure
2
2
Obstruction of Flow
2
2
Insufficient Flow or Under Infusion
2
2
Device Contamination with Chemical or Other Material
2
2
Malposition of Device
2
2
Difficult or Delayed Positioning
2
2
Temperature Problem
2
2
Overheating of Device
1
1
Human-Device Interface Problem
1
1
Deformation Due to Compressive Stress
1
1
Protective Measures Problem
1
1
Failure to Advance
1
1
Pacing Problem
1
1
Component Misassembled
1
1
Output below Specifications
1
1
Inadequacy of Device Shape and/or Size
1
1
Retraction Problem
1
1
High Test Results
1
1
Infusion or Flow Problem
1
1
Material Twisted/Bent
1
1
Gas/Air Leak
1
1
Positioning Failure
1
1
No Pressure
1
1
Contamination /Decontamination Problem
1
1
Therapeutic or Diagnostic Output Failure
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
143
143
No Consequences Or Impact To Patient
90
90
No Known Impact Or Consequence To Patient
45
45
Insufficient Information
12
12
Hemorrhage/Bleeding
11
11
Blood Loss
5
5
Hypersensitivity/Allergic reaction
4
4
Foreign Body In Patient
4
4
No Patient Involvement
4
4
Low Blood Pressure/ Hypotension
4
4
Unspecified Infection
3
4
Shaking/Tremors
3
3
Perforation of Vessels
3
3
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
2
2
Perforation
2
2
Fever
2
2
Chills
2
2
High Blood Pressure/ Hypertension
1
1
Arrhythmia
1
1
No Code Available
1
1
Respiratory Distress
1
1
No Information
1
1
Hemoptysis
1
1
Alteration In Body Temperature
1
1
Cardiac Arrest
1
1
Ventricular Fibrillation
1
1
Needle Stick/Puncture
1
1
Cardiac Perforation
1
1
Thrombosis
1
1
Reaction
1
1
Swelling/ Edema
1
1
Tachycardia
1
1
Thrombus
1
1
Hemothorax
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Edwards Lifesciences, LLC
II
Aug-12-2021
2
Edwards Lifesciences, LLC
II
Jul-10-2020
3
ICU Medical, Inc.
II
May-14-2020
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