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TPLC
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Device
catheter, umbilical artery
Product Code
FOS
Regulation Number
880.5200
Device Class
2
Premarket Reviews
Manufacturer
Decision
COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
SUBSTANTIALLY EQUIVALENT
1
FOOTPRINT MEDICAL
SUBSTANTIALLY EQUIVALENT
2
FOOTPRINT MEDICAL INC.
SUBSTANTIALLY EQUIVALENT
1
HAOLANG MEDICAL USA CORPORATION
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2014
69
69
2015
81
81
2016
115
115
2017
139
139
2018
84
84
2019
64
64
2020
43
43
2021
49
49
2022
38
38
2023
20
20
2024
34
34
Device Problems
MDRs with this Device Problem
Events in those MDRs
Leak/Splash
219
219
Fluid/Blood Leak
200
200
Break
131
131
Crack
92
92
Hole In Material
27
27
Material Fragmentation
17
17
Connection Problem
16
16
Fracture
14
14
Material Puncture/Hole
13
13
Air Leak
10
10
Detachment of Device or Device Component
10
10
Adverse Event Without Identified Device or Use Problem
8
8
Malposition of Device
8
8
Material Split, Cut or Torn
8
8
Complete Blockage
7
7
Defective Device
7
7
Positioning Problem
7
7
Device Operates Differently Than Expected
7
7
Migration
7
7
Detachment Of Device Component
7
7
Use of Device Problem
7
7
Backflow
7
7
Obstruction of Flow
7
7
Infusion or Flow Problem
6
6
Material Separation
6
6
Difficult to Remove
6
6
Material Integrity Problem
5
5
Entrapment of Device
5
5
Device Markings/Labelling Problem
5
5
Split
5
5
Bent
5
5
Improper Flow or Infusion
5
5
Insufficient Information
4
4
Migration or Expulsion of Device
4
4
Appropriate Term/Code Not Available
4
4
Improper or Incorrect Procedure or Method
4
4
Patient Device Interaction Problem
4
4
Disconnection
4
4
Material Perforation
3
3
Air/Gas in Device
3
3
Structural Problem
2
2
Reflux within Device
2
2
Device Displays Incorrect Message
2
2
Device Dislodged or Dislocated
2
2
Material Deformation
2
2
Material Rupture
2
2
Gas/Air Leak
2
2
Occlusion Within Device
2
2
Difficult to Insert
2
2
Moisture Damage
2
2
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Known Impact Or Consequence To Patient
274
274
No Consequences Or Impact To Patient
123
123
No Clinical Signs, Symptoms or Conditions
82
82
No Information
60
60
Foreign Body In Patient
26
26
Hemorrhage/Bleeding
26
26
Blood Loss
25
25
Insufficient Information
24
24
Device Embedded In Tissue or Plaque
23
23
No Code Available
18
18
Death
12
12
No Patient Involvement
11
11
Pericardial Effusion
6
6
Air Embolism
6
6
Extravasation
5
5
Abdominal Distention
4
4
Low Blood Pressure/ Hypotension
3
3
Ischemia
3
3
Sepsis
3
3
Pleural Effusion
3
3
Fluid Discharge
3
3
Hypoglycemia
3
3
Cardiac Tamponade
2
2
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
2
2
Discomfort
2
2
Liver Contusion
2
2
Pain
2
2
Shock
2
2
Perforation of Vessels
2
2
Low Oxygen Saturation
1
1
Internal Organ Perforation
1
1
Ascites
1
1
Bacterial Infection
1
1
Irritability
1
1
Lethargy
1
1
Distress
1
1
Infiltration into Tissue
1
1
Extubate
1
1
Liver Laceration(s)
1
1
Angioedema
1
1
Skin Tears
1
1
Swelling/ Edema
1
1
Tachycardia
1
1
Renal Failure
1
1
Unspecified Kidney or Urinary Problem
1
1
Cardiogenic Shock
1
1
Septic Shock
1
1
Vomiting
1
1
Intracranial Hemorrhage
1
1
Injury
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Cardinal Health 200, LLC
I
Aug-13-2021
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