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TPLC
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Device
adaptor, stopcock, manifold, fitting, cardiopulmonary bypass
Product Code
DTL
Regulation Number
870.4290
Device Class
2
Premarket Reviews
Manufacturer
Decision
COEUR, INC.
SUBSTANTIALLY EQUIVALENT
1
EDWARDS LIFESCIENCES, LLC.
SUBSTANTIALLY EQUIVALENT
1
GALT MEDICAL CORP.
SUBSTANTIALLY EQUIVALENT
1
JILIN CORONADO MEDICAL LTD.
SUBSTANTIALLY EQUIVALENT
1
MEDLINE INDUSTRIES, INC.
SUBSTANTIALLY EQUIVALENT
1
MEDTRONIC INC.
SUBSTANTIALLY EQUIVALENT
3
MERIT MEDICAL SYSTEMS, INC.
SUBSTANTIALLY EQUIVALENT
3
NAVILYST MEDICAL, INC.
SUBSTANTIALLY EQUIVALENT
1
SHANGHAI KINDLY MEDICAL INSTRUMENTS CO.,LTD.
SUBSTANTIALLY EQUIVALENT
1
SYNEXMED(SHENZHEN)COMPANY LIMITED
SUBSTANTIALLY EQUIVALENT
1
TERUMO CARDIOVASCULAR SYSTEMS CORPORATION
SUBSTANTIALLY EQUIVALENT
1
VASCULAR SOLUTIONS ZERUSA LTD.
SUBSTANTIALLY EQUIVALENT
1
VASCULAR SOLUTIONS, INC.
SUBSTANTIALLY EQUIVALENT
1
ZERUSA LIMITED
SUBSTANTIALLY EQUIVALENT
2
MDR Year
MDR Reports
MDR Events
2014
80
80
2015
89
89
2016
67
67
2017
106
106
2018
84
84
2019
76
76
2020
53
53
2021
55
55
2022
48
48
2023
46
46
2024
276
276
Device Problems
MDRs with this Device Problem
Events in those MDRs
Leak/Splash
405
405
Human-Device Interface Problem
123
123
Loose or Intermittent Connection
76
76
Air/Gas in Device
51
51
Hole In Material
29
29
Fluid/Blood Leak
28
28
Tear, Rip or Hole in Device Packaging
27
27
Improper or Incorrect Procedure or Method
20
20
Unable to Obtain Readings
19
19
Infusion or Flow Problem
18
18
Display or Visual Feedback Problem
17
17
Air Leak
16
16
Device Contamination with Chemical or Other Material
16
16
Crack
15
15
Break
12
12
Detachment Of Device Component
11
11
Suction Problem
11
11
Device Markings/Labelling Problem
10
10
Physical Resistance/Sticking
10
10
Defective Device
9
9
Device Operates Differently Than Expected
8
8
Adverse Event Without Identified Device or Use Problem
8
8
Gas/Air Leak
7
7
Physical Resistance
7
7
Fitting Problem
7
7
Inflation Problem
7
7
Failure to Cycle
6
6
Delivered as Unsterile Product
6
6
Improper Device Output
6
6
Material Deformation
6
6
No Flow
6
6
Material Integrity Problem
5
5
Device Packaging Compromised
5
5
Device-Device Incompatibility
5
5
Difficult to Advance
5
5
Difficult to Insert
5
5
Difficult to Remove
4
4
Fracture
4
4
Deflation Problem
4
4
Connection Problem
4
4
Device Disinfection Or Sterilization Issue
4
4
Use of Device Problem
4
4
Unstable
3
3
Contamination /Decontamination Problem
3
3
Detachment of Device or Device Component
3
3
Improper Flow or Infusion
3
3
Material Puncture/Hole
3
3
Product Quality Problem
3
3
Mechanical Problem
3
3
Unsealed Device Packaging
3
3
Therapeutic or Diagnostic Output Failure
3
3
No Apparent Adverse Event
3
3
Pressure Problem
2
2
Suction Failure
2
2
Noise, Audible
2
2
Material Split, Cut or Torn
2
2
Difficult To Position
2
2
Device Difficult to Setup or Prepare
2
2
Material Separation
2
2
Problem with Sterilization
2
2
Device Contaminated During Manufacture or Shipping
2
2
Insufficient Flow or Under Infusion
2
2
Component Missing
2
2
Device Contamination with Body Fluid
1
1
Other (for use when an appropriate device code cannot be identified)
1
1
Device Damaged Prior to Use
1
1
Failure to Zero
1
1
Implant Mobility NOS (Not otherwise specified)
1
1
Malfunction
1
1
Obstruction of Flow
1
1
Failure to Advance
1
1
Separation Failure
1
1
Mechanical Jam
1
1
Difficult to Open or Close
1
1
Filtration Problem
1
1
Device Inoperable
1
1
Device Slipped
1
1
Incorrect, Inadequate or Imprecise Result or Readings
1
1
Off-Label Use
1
1
Kinked
1
1
Disconnection
1
1
Difficult to Flush
1
1
Flushing Problem
1
1
Excess Flow or Over-Infusion
1
1
Decoupling
1
1
Bent
1
1
Backflow
1
1
Contamination
1
1
Corroded
1
1
Patient Device Interaction Problem
1
1
Output Problem
1
1
Packaging Problem
1
1
Insufficient Information
1
1
Appropriate Term/Code Not Available
1
1
Missing Value Reason
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
392
392
No Consequences Or Impact To Patient
233
233
Blood Loss
115
115
No Known Impact Or Consequence To Patient
85
85
No Patient Involvement
62
62
Air Embolism
30
30
Not Applicable
24
24
No Information
18
18
Insufficient Information
17
17
Cardiac Arrest
9
9
Injury
6
6
Hemorrhage/Bleeding
4
4
Low Blood Pressure/ Hypotension
4
4
Non specific EKG/ECG Changes
2
2
Embolism
2
2
ST Segment Elevation
2
2
Bradycardia
2
2
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
1
1
Collapse
1
1
Obstruction/Occlusion
1
1
Respiratory Failure
1
1
No Patient involvement
1
1
Patient Problem/Medical Problem
1
1
Thrombus
1
1
Ventricular Fibrillation
1
1
Ventricular Tachycardia
1
1
Discomfort
1
1
Myocardial Infarction
1
1
Overdose
1
1
Perforation
1
1
Death
1
1
Arrhythmia
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Abbott Vascular
II
Jul-12-2011
2
Boston Scientific Corporation
II
May-16-2023
3
Cook Inc.
II
May-09-2018
4
Dokitz NovoSci
II
Nov-06-2014
5
Edwards Lifesciences Llc
II
Dec-07-2010
6
LivaNova USA Inc.
III
Jul-17-2020
7
LivaNova USA Inc.
II
Jun-26-2020
8
Medline Industries Inc
II
Sep-24-2021
9
Medtronic Perfusion Systems
II
Jul-10-2017
10
Merit Medical Systems, Inc.
II
Apr-11-2022
11
Sorin Group USA, Inc.
II
Oct-25-2012
12
Terumo Cardiovascular Systems Corp
II
Jun-23-2015
13
Terumo Cardiovascular Systems Corporation
II
Jun-21-2018
14
Thomas Medical Products Inc
II
Feb-14-2011
15
Vascular Solutions, Inc.
I
Apr-07-2016
16
Vascular Solutions, Inc.
I
Mar-20-2013
17
Vascular Solutions, Inc.
II
Sep-17-2012
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