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TPLC
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Device
pump, blood, cardiopulmonary bypass, non-roller type
Product Code
KFM
Regulation Number
870.4360
Device Class
2
Premarket Reviews
Manufacturer
Decision
CARDIACASSIST INC
SUBSTANTIALLY EQUIVALENT
1
CARDIACASSIST, INC.
SUBSTANTIALLY EQUIVALENT
1
INTERNATIONAL BIOPHYSICS CORPORATION
SUBSTANTIALLY EQUIVALENT
1
MEDTRONIC INC
SUBSTANTIALLY EQUIVALENT
1
MEDTRONIC, INC.
SUBSTANTIALLY EQUIVALENT
1
QURA S.R.L
SUBSTANTIALLY EQUIVALENT
1
1. K192850
Quantum PureFlow Centrifugal Blood Pump CP37, Quan
...
2. K201320
Quantum PureFlow Centrifugal Blood Pump CP22 with
...
3. K220842
Quantum Perfusion Centrifugal Blood Pump CP22 with
...
4. K233091
Quantum Perfusion Centrifugal Blood Pump CP37 with
...
QURA S.R.L.
SUBSTANTIALLY EQUIVALENT
4
1. K192850
Quantum PureFlow Centrifugal Blood Pump CP37, Quan
...
2. K201320
Quantum PureFlow Centrifugal Blood Pump CP22 with
...
3. K220842
Quantum Perfusion Centrifugal Blood Pump CP22 with
...
4. K233091
Quantum Perfusion Centrifugal Blood Pump CP37 with
...
SORIN GROUP ITALIA S.R.L.
SUBSTANTIALLY EQUIVALENT
1
TERUMO CARDIOVASCULAR SYSTEMS CORPORATION
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2019
310
310
2020
438
438
2021
447
447
2022
294
294
2023
354
354
2024
114
114
Device Problems
MDRs with this Device Problem
Events in those MDRs
Electrical /Electronic Property Problem
334
334
Insufficient Information
226
226
Adverse Event Without Identified Device or Use Problem
182
182
Noise, Audible
174
174
Pumping Stopped
168
168
Infusion or Flow Problem
121
121
Device Displays Incorrect Message
119
119
Mechanical Problem
112
112
Overheating of Device
88
88
Battery Problem
74
74
Unexpected Shutdown
72
72
Communication or Transmission Problem
47
47
Pumping Problem
35
35
Inaccurate Flow Rate
33
33
No Flow
26
26
Decreased Pump Speed
25
25
Insufficient Flow or Under Infusion
22
22
Fluid/Blood Leak
21
21
Increased Pump Speed
17
17
No Apparent Adverse Event
17
17
No Display/Image
17
17
Material Twisted/Bent
16
16
Excessive Heating
16
16
Break
15
15
Display or Visual Feedback Problem
14
14
Disconnection
14
14
Device Difficult to Setup or Prepare
13
13
Obstruction of Flow
12
12
Electrical Power Problem
12
12
Use of Device Problem
11
11
Leak/Splash
11
11
Crack
10
10
Failure to Pump
10
10
Power Problem
10
10
Failure to Power Up
9
9
Premature Discharge of Battery
8
8
Connection Problem
7
7
Product Quality Problem
7
7
Vibration
7
7
Detachment of Device or Device Component
7
7
Loose or Intermittent Connection
7
7
Improper Flow or Infusion
6
6
Loss of Power
6
6
Fitting Problem
6
6
Unexpected Therapeutic Results
6
6
Fracture
6
6
Charging Problem
5
5
Material Deformation
5
5
Temperature Problem
5
5
Erratic or Intermittent Display
5
5
Device Alarm System
5
5
Labelling, Instructions for Use or Training Problem
4
4
Pressure Problem
4
4
Device Sensing Problem
4
4
Gas/Air Leak
4
4
Material Puncture/Hole
4
4
Appropriate Term/Code Not Available
4
4
Therapeutic or Diagnostic Output Failure
3
3
Failure to Deliver
3
3
Decoupling
3
3
Failure to Read Input Signal
3
3
Defective Component
3
3
No Visual Prompts/Feedback
3
3
Physical Resistance/Sticking
3
3
Image Display Error/Artifact
3
3
Electrical Shorting
3
3
Protective Measures Problem
3
3
Misassembly by Users
3
3
Inaccurate Delivery
3
3
Incorrect, Inadequate or Imprecise Result or Readings
3
3
Manufacturing, Packaging or Shipping Problem
3
3
Unable to Obtain Readings
2
2
Complete Loss of Power
2
2
Failure to Shut Off
2
2
Failure to Align
2
2
Nonstandard Device
2
2
Partial Blockage
2
2
Alarm Not Visible
2
2
Air/Gas in Device
2
2
Material Integrity Problem
2
2
Visual Prompts will not Clear
2
2
Gradient Increase
2
2
No Audible Alarm
2
2
Particulates
2
2
High Readings
2
2
Contamination /Decontamination Problem
2
2
Backflow
2
2
Coagulation in Device or Device Ingredient
2
2
Intermittent Communication Failure
1
1
Failure to Run on Battery
1
1
Smoking
1
1
Shipping Damage or Problem
1
1
Inadequate Instructions for Healthcare Professional
1
1
Material Split, Cut or Torn
1
1
Fire
1
1
Expiration Date Error
1
1
Failure to Prime
1
1
Failure to Cycle
1
1
Display Difficult to Read
1
1
Migration
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
983
983
No Consequences Or Impact To Patient
281
281
No Patient Involvement
205
205
No Known Impact Or Consequence To Patient
175
175
Insufficient Information
93
93
Hemorrhage/Bleeding
63
63
Thrombosis/Thrombus
42
42
Death
42
42
Hemolysis
35
35
Cardiac Arrest
31
31
Heart Failure/Congestive Heart Failure
25
25
No Information
22
22
Thrombus
21
21
Low Oxygen Saturation
19
19
Bacterial Infection
17
17
Arrhythmia
17
17
Renal Failure
16
16
Thromboembolism
14
14
Blood Loss
13
13
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
12
12
Ischemia Stroke
12
12
Stroke/CVA
11
11
Multiple Organ Failure
11
11
Respiratory Failure
11
11
Hypoxia
11
11
Unspecified Infection
11
11
Cardiogenic Shock
10
10
Atrial Fibrillation
10
10
Low Blood Pressure/ Hypotension
10
10
Tachycardia
10
10
Sepsis
8
8
Renal Impairment
8
8
Hematoma
7
7
Intracranial Hemorrhage
6
6
Anemia
6
6
Hemorrhagic Stroke
5
5
Gastrointestinal Hemorrhage
5
5
Fungal Infection
5
5
Hematuria
4
4
Air Embolism
4
4
Ventricular Fibrillation
4
4
Dyspnea
4
4
Respiratory Insufficiency
4
4
Bradycardia
4
4
Brain Injury
4
4
Right Ventricular Failure
4
4
Reaction
4
4
Lactate Dehydrogenase Increased
4
4
Ischemia
4
4
Hemothorax
3
3
Shock
3
3
Septic Shock
3
3
Thrombosis
3
3
Obstruction/Occlusion
3
3
Liver Damage/Dysfunction
3
3
Liver Failure
3
3
Hypovolemia
3
3
Pain
3
3
Encephalopathy
3
3
High Blood Pressure/ Hypertension
3
3
Cardiac Tamponade
2
2
Cardiopulmonary Arrest
2
2
Unspecified Gastrointestinal Problem
2
2
Melena
2
2
Aspiration Pneumonitis
2
2
Kidney Infection
2
2
Coagulation Disorder
2
2
Epistaxis
2
2
Convulsion/Seizure
2
2
Thrombocytopenia
2
2
No Code Available
2
2
Hydrocephalus
2
2
Visual Impairment
2
2
Complaint, Ill-Defined
2
2
Pleural Effusion
2
2
Drug Resistant Bacterial Infection
2
2
Muscle Weakness
2
2
Cough
1
1
Failure of Implant
1
1
Coma
1
1
Sleep Dysfunction
1
1
Emotional Changes
1
1
Tricuspid Valve Insufficiency/ Regurgitation
1
1
Hypervolemia
1
1
Aortic Valve Insufficiency/ Regurgitation
1
1
Cerebral Edema
1
1
Anxiety
1
1
Respiratory Distress
1
1
Heart Failure
1
1
Peripheral Edema
1
1
Respiratory Arrest
1
1
Confusion/ Disorientation
1
1
Irritability
1
1
Asystole
1
1
Hemorrhage, Cerebral
1
1
Atrial Flutter
1
1
Embolism/Embolus
1
1
Inflammation
1
1
Valvular Insufficiency/ Regurgitation
1
1
Pancreatitis
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Cardiac Assist, Inc
II
Aug-25-2023
2
Cardiac Assist, Inc
II
May-11-2020
3
Maquet Cardiovascular Us Sales, Llc
III
Sep-12-2020
4
Maquet Cardiovascular Us Sales, Llc
II
Dec-12-2019
5
Maquet Medical Systems USA
II
Feb-02-2024
6
OriGen Biomedical, Inc.
II
Oct-30-2020
7
QURA S.R.L.
II
Aug-12-2021
8
Thoratec Switzerland GMBH
I
Oct-30-2019
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