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Device
console, heart-lung machine, cardiopulmonary bypass
Regulation Description
Cardiopulmonary bypass heart-lung machine console.
Product Code
DTQ
Regulation Number
870.4220
Device Class
2
Premarket Reviews
Manufacturer
Decision
CENTURY HLM, LLC
SUBSTANTIALLY EQUIVALENT
1
LIVANOVA DEUTSCHLAND, GMBH
SUBSTANTIALLY EQUIVALENT
3
TERUMO CARDIOVASCULAR SYSTEMS CORPORATION
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2020
627
627
2021
729
731
2022
717
719
2023
818
838
2024
863
865
2025
936
971
Device Problems
MDRs with this Device Problem
Events in those MDRs
Output Problem
669
669
Pumping Problem
522
533
Pumping Stopped
465
481
Display or Visual Feedback Problem
272
272
Difficult to Open or Close
254
254
Device Alarm System
232
232
Mechanical Problem
193
195
Pressure Problem
172
172
Calibration Problem
141
141
Incorrect, Inadequate or Imprecise Result or Readings
135
135
Failure to Calibrate
123
123
Infusion or Flow Problem
119
121
Communication or Transmission Problem
115
116
Electrical /Electronic Property Problem
103
103
Device Sensing Problem
96
97
Failure to Read Input Signal
95
95
Power Problem
94
94
Break
77
77
Battery Problem
75
76
Charging Problem
70
70
No Display/Image
68
68
Inadequate User Interface
63
63
Failure to Pump
62
62
Failure to Power Up
62
62
False Alarm
47
47
No Flow
44
44
Application Program Problem
42
42
Insufficient Information
39
39
Low Readings
38
39
Connection Problem
36
36
Adverse Event Without Identified Device or Use Problem
35
35
Unable to Obtain Readings
35
35
Unexpected Shutdown
34
34
Crack
25
25
Material Deformation
25
25
Mechanical Jam
24
24
Defective Alarm
23
23
Improper Flow or Infusion
22
22
Loss of or Failure to Bond
22
22
Decoupling
22
22
Noise, Audible
22
23
Application Program Freezes, Becomes Nonfunctional
21
21
Computer Software Problem
18
18
Detachment of Device or Device Component
18
18
Incorrect Measurement
18
18
Failure to Auto Stop
17
17
Increase in Pressure
15
15
Use of Device Problem
14
14
Overheating of Device
14
14
Circuit Failure
13
13
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
3829
3890
No Consequences Or Impact To Patient
399
399
Insufficient Information
283
283
No Patient Involvement
204
204
No Known Impact Or Consequence To Patient
77
77
Cardiac Arrest
43
43
Hemorrhage/Bleeding
16
16
Death
11
11
Air Embolism
10
10
Low Oxygen Saturation
10
10
Arrhythmia
8
8
Low Blood Pressure/ Hypotension
7
7
Asystole
6
6
Bronchial Hemorrhage
4
4
Brain Injury
4
4
Exsanguination
4
4
Bone Fracture(s)
4
4
Hemolysis
3
3
Hypoxia
3
3
Hemothorax
2
2
Nervous System Injury
2
2
Airway Obstruction
2
2
Aneurysm
2
2
Cardiovascular Insufficiency
2
2
Pulmonary Edema
2
2
Tachycardia
2
2
Heart Failure/Congestive Heart Failure
2
2
Bradycardia
2
2
Valvular Stenosis
2
2
Septic Shock
2
2
Intracranial Hemorrhage
2
2
Burn(s)
2
2
Myocarditis
2
2
Multiple Organ Failure
2
2
Blood Loss
2
2
Ischemia
2
2
Hematoma
2
2
Sepsis
2
2
Respiratory Arrest
2
2
Thrombosis/Thrombus
1
1
Hemolytic Anemia
1
1
Low Cardiac Output
1
1
Embolism/Embolus
1
1
Bacterial Infection
1
1
Shock from Patient Lead(s)
1
1
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
1
1
Ischemia Stroke
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
LivaNova Deutschland GmbH
II
Nov-27-2024
2
LivaNova USA Inc.
III
Feb-10-2020
3
Maquet Cardiopulmonary Ag
II
May-27-2025
4
Maquet Medical Systems USA
III
Sep-30-2024
5
Maquet Medical Systems USA
II
May-16-2024
6
Maquet Medical Systems USA
II
Feb-08-2024
7
Maquet Medical Systems USA
II
Dec-21-2023
8
Maquet Medical Systems USA
II
Dec-14-2023
9
Maquet Medical Systems USA
I
Dec-07-2023
10
Maquet Medical Systems USA
II
Nov-09-2023
11
Maquet Medical Systems USA
II
May-26-2023
12
Maquet Medical Systems USA
II
Apr-08-2022
13
Spectrum Medical Ltd.
II
Oct-24-2024
14
Terumo Cardiovascular Systems Corporation
II
Aug-26-2021
15
Terumo Cardiovascular Systems Corporation
II
Sep-12-2020
16
Terumo Cardiovascular Systems Corporation
II
Feb-07-2020
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