Quick Links: Skip to main page content
Skip to Search
Skip to Topics Menu
Skip to Common Links
U.S. Food & Drug Administration
Follow FDA
En Español
Search FDA
Home
Food
Drugs
Medical Devices
Radiation-Emitting Products
Vaccines, Blood & Biologics
Animal & Veterinary
Cosmetics
Tobacco Products
TPLC - Total Product Life Cycle
FDA Home
medical devices
databases
-
510(k)
|
DeNovo
|
Registration & Listing
|
Adverse Events
|
Recalls
|
PMA
|
HDE
|
Classification
|
Standards
CFR Title 21
|
Radiation-Emitting Products
|
X-Ray Assembler
|
Medsun Reports
|
CLIA
|
TPLC
New Search
show TPLC since
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
Back to Search Results
Device
apparatus, autotransfusion
Product Code
CAC
Regulation Number
868.5830
Device Class
2
Premarket Reviews
Manufacturer
Decision
ATRIUM MEDICAL CORPORATION
SUBSTANTIALLY EQUIVALENT
1
FRESENIUS KABI AG
SUBSTANTIALLY EQUIVALENT
4
HAEMONETICS CORP.
SUBSTANTIALLY EQUIVALENT
3
HAEMONETICS CORPORATION
SUBSTANTIALLY EQUIVALENT
3
INARI MEDICAL
SUBSTANTIALLY EQUIVALENT
1
INARI MEDICAL, INC.
SUBSTANTIALLY EQUIVALENT
2
MEDTRONIC INC.
SUBSTANTIALLY EQUIVALENT
1
MEDTRONIC PERFUSION SYSTEMS
SUBSTANTIALLY EQUIVALENT
1
PROCELL SURGICAL, INC.
SUBSTANTIALLY EQUIVALENT
1
SISU GLOBAL HEALTH
SUBSTANTIALLY EQUIVALENT
1
SORIN GROUP DEUTSCHLAND GMBH
SUBSTANTIALLY EQUIVALENT
1
SORIN GROUP ITALIA S.R.L
SUBSTANTIALLY EQUIVALENT
1
SORIN GROUP ITALIA S.R.L.
SUBSTANTIALLY EQUIVALENT
4
TELEFLEX MEDICAL, INC.
SUBSTANTIALLY EQUIVALENT
3
TLELFLEX MEDICAL, INC.
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2014
90
90
2015
87
87
2016
73
73
2017
88
88
2018
87
87
2019
64
64
2020
108
108
2021
73
73
2022
65
65
2023
39
39
2024
21
21
Device Problems
MDRs with this Device Problem
Events in those MDRs
Fluid/Blood Leak
113
113
Crack
90
90
Leak/Splash
50
50
Infusion or Flow Problem
40
40
Device Operates Differently Than Expected
39
39
Insufficient Information
34
34
Suction Problem
34
34
Break
33
33
Material Integrity Problem
31
31
Adverse Event Without Identified Device or Use Problem
30
30
Nonstandard Device
25
25
Mechanical Problem
24
24
Disconnection
23
23
Air Leak
18
18
Device Misassembled During Manufacturing /Shipping
15
15
Improper or Incorrect Procedure or Method
14
14
Obstruction of Flow
14
14
Deformation Due to Compressive Stress
13
13
Gas/Air Leak
12
12
Coagulation in Device or Device Ingredient
12
12
Other (for use when an appropriate device code cannot be identified)
11
11
Material Deformation
11
11
Device Displays Incorrect Message
10
10
Noise, Audible
9
9
Material Puncture/Hole
9
9
Difficult to Remove
9
9
Detachment Of Device Component
9
9
Decrease in Pressure
8
8
Defective Component
8
8
Component Missing
8
8
Electrical /Electronic Property Problem
7
7
Appropriate Term/Code Not Available
7
7
Connection Problem
7
7
Device Alarm System
6
6
Thermal Decomposition of Device
6
6
Device Inoperable
6
6
Use of Device Problem
5
5
Kinked
5
5
Loose or Intermittent Connection
5
5
Detachment of Device or Device Component
5
5
Contamination /Decontamination Problem
5
5
Device Contamination with Body Fluid
5
5
Tear, Rip or Hole in Device Packaging
5
5
No Apparent Adverse Event
5
5
No Flow
4
4
Material Twisted/Bent
4
4
Therapeutic or Diagnostic Output Failure
4
4
Overfill
4
4
Defective Device
4
4
Difficult to Open or Close
4
4
Device Contamination with Chemical or Other Material
4
4
Hole In Material
4
4
Disassembly
4
4
Unsealed Device Packaging
4
4
Smoking
4
4
Inadequate Filtration Process
4
4
Insufficient Flow or Under Infusion
4
4
Vibration
3
3
Failure to Power Up
3
3
Device Emits Odor
3
3
Device Slipped
3
3
Material Discolored
3
3
Excess Flow or Over-Infusion
3
3
Burst Container or Vessel
3
3
Decrease in Suction
3
3
Manufacturing, Packaging or Shipping Problem
3
3
Device Issue
3
3
Biocompatibility
3
3
Physical Resistance/Sticking
3
3
Pressure Problem
2
2
Optical Problem
2
2
Improper Device Output
2
2
Device Packaging Compromised
2
2
Computer Operating System Problem
2
2
Entrapment of Device
2
2
Fracture
2
2
Partial Blockage
2
2
Fire
2
2
Delivered as Unsterile Product
2
2
Occlusion Within Device
2
2
Misconnection
2
2
Self-Activation or Keying
2
2
Device Stops Intermittently
2
2
Out-Of-Box Failure
2
2
Invalid Sensing
1
1
Microbial Contamination of Device
1
1
Fitting Problem
1
1
Device Damaged Prior to Use
1
1
Increase in Suction
1
1
Inadequate or Insufficient Training
1
1
Volume Accuracy Problem
1
1
Material Separation
1
1
Inappropriate/Inadequate Shock/Stimulation
1
1
Inadequacy of Device Shape and/or Size
1
1
Incorrect, Inadequate or Imprecise Result or Readings
1
1
No Device Output
1
1
Overheating of Device
1
1
Off-Label Use
1
1
Product Quality Problem
1
1
Reflux within Device
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Known Impact Or Consequence To Patient
182
182
No Clinical Signs, Symptoms or Conditions
161
161
No Consequences Or Impact To Patient
141
141
No Information
64
64
No Patient Involvement
48
48
Blood Loss
30
30
Hemorrhage/Bleeding
28
28
Pneumothorax
25
25
No Code Available
19
19
Death
16
16
Insufficient Information
14
14
Device Embedded In Tissue or Plaque
12
12
Unspecified Blood or Lymphatic problem
12
12
Foreign Body In Patient
6
6
Cardiac Arrest
6
6
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
5
5
Hypovolemia
4
4
Therapeutic Response, Decreased
4
4
Complaint, Ill-Defined
4
4
Low Blood Pressure/ Hypotension
4
4
Hemolysis
4
4
Pleural Effusion
4
4
Pain
3
3
Low Oxygen Saturation
3
3
Not Applicable
3
3
Thrombosis/Thrombus
2
2
Reaction
2
2
Other (for use when an appropriate patient code cannot be identified)
2
2
Respiratory Distress
2
2
Sepsis
2
2
Dyspnea
2
2
Hematoma
2
2
Exposure to Body Fluids
2
2
Pulmonary Embolism
2
2
Abscess
1
1
Adult Respiratory Distress Syndrome
1
1
Air Embolism
1
1
Bradycardia
1
1
Cardiopulmonary Arrest
1
1
Chest Pain
1
1
Disseminated Intravascular Coagulation (DIC)
1
1
Hypoxia
1
1
Unspecified Infection
1
1
Inflammation
1
1
Therapeutic Effects, Unexpected
1
1
Thrombus
1
1
Transient Ischemic Attack
1
1
Venipuncture
1
1
Dizziness
1
1
Brain Injury
1
1
Pneumonia
1
1
Hemothorax
1
1
Pulmonary Edema
1
1
Local Reaction
1
1
Renal Failure
1
1
Loss of consciousness
1
1
Chest Tightness/Pressure
1
1
No Patient involvement
1
1
Lead(s), Burn(s) From
1
1
Sudden Cardiac Death
1
1
Skin Tears
1
1
Cognitive Changes
1
1
Injury
1
1
Impaired Healing
1
1
Extubate
1
1
Aspiration Pneumonitis
1
1
Cough
1
1
Blister
1
1
Ruptured Aneurysm
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Atrium Medical Corporation
II
Dec-28-2023
2
Atrium Medical Corporation
II
Dec-02-2023
3
Atrium Medical Corporation
II
Nov-16-2023
4
Atrium Medical Corporation
II
Feb-15-2017
5
Atrium Medical Corporation
II
Jul-01-2014
6
Atrium Medical Corporation
II
Jan-14-2014
7
Fenwal Inc
II
Apr-23-2019
8
Fenwal Inc
II
Mar-26-2019
9
Fresenius Kabi, LLC
II
Nov-10-2010
10
Haemonetics Corporation
II
Jan-29-2020
11
Haemonetics Corporation
II
Jan-28-2019
12
Haemonetics Corporation
II
Aug-30-2018
13
Haemonetics Corporation
II
Aug-05-2011
14
Haemonetics Corporation
II
Jun-07-2011
15
Haemonetics Corporation
II
Feb-22-2011
16
Maquet Cardiovascular, LLC
I
Jan-12-2024
17
Medtronic Perfusion Systems
II
Jan-29-2019
18
Stryker Instruments Div. of Stryker Corporation
II
May-01-2015
19
Stryker Instruments Div. of Stryker Corporation
II
Jan-29-2010
20
Teleflex Medical
II
Apr-28-2016
-
-