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TPLC
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Device
catheter, nephrostomy
Product Code
LJE
Device Class
Unclassified
Premarket Reviews
Manufacturer
Decision
BOSTON SCIENTIFIC CORP.
SUBSTANTIALLY EQUIVALENT
1
BOSTON SCIENTIFIC CORPORATION
SUBSTANTIALLY EQUIVALENT
1
COLOPLAST CORP
SUBSTANTIALLY EQUIVALENT - KIT
2
COOK INCORPORATED
SUBSTANTIALLY EQUIVALENT
4
SUBSTANTIALLY EQUIVALENT - KIT
4
GYRUS ACMI, INC.
SUBSTANTIALLY EQUIVALENT
1
JBW7 INNOVATIONS, LLC
SUBSTANTIALLY EQUIVALENT
1
YOUCARE TECHNOLOGY CO., LTD. (WUHAN)
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2014
4
4
2015
9
9
2016
26
26
2017
60
60
2018
69
69
2019
78
78
2020
50
50
2021
38
38
2022
42
42
2023
132
132
2024
6
6
Device Problems
MDRs with this Device Problem
Events in those MDRs
Burst Container or Vessel
73
73
Adverse Event Without Identified Device or Use Problem
63
63
Material Rupture
59
59
Fluid/Blood Leak
45
45
Break
35
35
Leak/Splash
34
34
Difficult to Remove
25
25
Material Separation
21
21
Fracture
18
18
Device Contamination with Chemical or Other Material
17
17
Detachment of Device or Device Component
16
16
Material Deformation
13
13
Inflation Problem
13
13
Difficult to Advance
12
12
Material Puncture/Hole
11
11
Material Fragmentation
9
9
Appropriate Term/Code Not Available
9
9
Material Split, Cut or Torn
9
9
Torn Material
7
7
Use of Device Problem
7
7
Obstruction of Flow
6
6
Material Integrity Problem
6
6
Material Twisted/Bent
5
5
Fitting Problem
5
5
Device Operates Differently Than Expected
5
5
Nonstandard Device
5
5
Difficult to Insert
4
4
Stretched
4
4
Deflation Problem
4
4
Detachment Of Device Component
4
4
Connection Problem
4
4
Defective Device
4
4
Device Dislodged or Dislocated
4
4
Entrapment of Device
3
3
Crack
3
3
Kinked
2
2
Unsealed Device Packaging
2
2
Product Quality Problem
2
2
Positioning Failure
2
2
Hole In Material
2
2
Complete Blockage
2
2
Difficult to Open or Remove Packaging Material
2
2
Device Contaminated During Manufacture or Shipping
2
2
Device Handling Problem
2
2
Tear, Rip or Hole in Device Packaging
2
2
Separation Failure
2
2
Deformation Due to Compressive Stress
2
2
Device Packaging Compromised
2
2
Component Missing
2
2
Out-Of-Box Failure
1
1
Failure to Infuse
1
1
Failure to Advance
1
1
Device Damaged Prior to Use
1
1
Retraction Problem
1
1
Malposition of Device
1
1
Migration
1
1
Pressure Problem
1
1
Therapeutic or Diagnostic Output Failure
1
1
Mechanical Jam
1
1
No Flow
1
1
Manufacturing, Packaging or Shipping Problem
1
1
Gas/Air Leak
1
1
Compatibility Problem
1
1
Difficult to Open or Close
1
1
Component Incompatible
1
1
Contamination
1
1
Calcified
1
1
Failure to Capture
1
1
Accessory Incompatible
1
1
Balloon rupture
1
1
Unintended Ejection
1
1
Mechanical Problem
1
1
Misassembled
1
1
Unraveled Material
1
1
Peeled/Delaminated
1
1
Difficult To Position
1
1
Decrease in Pressure
1
1
Inadequate Instructions for Healthcare Professional
1
1
Device Fell
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
142
142
No Consequences Or Impact To Patient
137
137
No Known Impact Or Consequence To Patient
85
85
No Code Available
58
58
Hemorrhage/Bleeding
19
19
Foreign Body In Patient
14
14
Sepsis
12
12
No Patient Involvement
12
12
Obstruction/Occlusion
10
10
No Information
10
10
Insufficient Information
10
10
Renal Failure
8
8
Urinary Tract Infection
6
6
Perforation
6
6
Tissue Damage
6
6
Septic Shock
5
5
Hematuria
4
4
Pain
4
4
Device Embedded In Tissue or Plaque
4
4
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
4
4
Pseudoaneurysm
3
3
Unspecified Infection
3
3
Blood Loss
3
3
Abscess
3
3
Fistula
2
2
Pneumonia
2
2
Pneumothorax
2
2
Hematoma
2
2
Respiratory Failure
2
2
Internal Organ Perforation
2
2
Pleural Effusion
2
2
Post Operative Wound Infection
2
2
Failure of Implant
2
2
Hypovolemic Shock
1
1
Perforation of Vessels
1
1
Unspecified Kidney or Urinary Problem
1
1
Anxiety
1
1
Hemothorax
1
1
Urinary Retention
1
1
Abdominal Pain
1
1
Unspecified Tissue Injury
1
1
Bowel Perforation
1
1
Pulmonary Embolism
1
1
Deposits
1
1
Fluid Discharge
1
1
Transient Ischemic Attack
1
1
Liver Damage/Dysfunction
1
1
Respiratory Insufficiency
1
1
Embolism
1
1
Cardiac Arrest
1
1
Purulent Discharge
1
1
Fever
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Boston Scientific Corporation
II
Jul-09-2013
2
C.R. Bard, Inc.
II
Nov-04-2016
3
Cook Inc.
II
Dec-22-2021
4
Cook Inc.
II
Oct-14-2020
5
Cook Inc.
II
Feb-04-2020
6
Cook Inc.
II
Mar-24-2016
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