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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
15
15
Device Problems
MDRs with this Device Problem
Events in those MDRs
Burst Container or Vessel
75
75
Adverse Event Without Identified Device or Use Problem
63
63
Material Rupture
59
59
Fluid/Blood Leak
45
45
Break
38
38
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
14
14
Inflation Problem
13
13
Difficult to Advance
12
12
Material Split, Cut or Torn
12
12
Material Puncture/Hole
11
11
Material Fragmentation
9
9
Appropriate Term/Code Not Available
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
Device Operates Differently Than Expected
5
5
Fitting Problem
5
5
Nonstandard Device
5
5
Difficult to Insert
4
4
Stretched
4
4
Deflation Problem
4
4
Detachment Of Device Component
4
4
Defective Device
4
4
Connection Problem
4
4
Device Dislodged or Dislocated
4
4
Device Contaminated During Manufacture or Shipping
3
3
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 Packaging Compromised
2
2
Deformation Due to Compressive Stress
2
2
Tear, Rip or Hole in Device Packaging
2
2
Separation Failure
2
2
Component Missing
2
2
Device Handling Problem
2
2
Physical Resistance/Sticking
2
2
Device Fell
1
1
Migration
1
1
Out-Of-Box Failure
1
1
Solder Joint Fracture
1
1
Failure to Infuse
1
1
Device Damaged Prior to Use
1
1
Retraction Problem
1
1
Failure to Advance
1
1
Malposition of Device
1
1
Difficult to Open or Close
1
1
Gas/Air Leak
1
1
Compatibility Problem
1
1
Manufacturing, Packaging or Shipping Problem
1
1
Pressure Problem
1
1
Therapeutic or Diagnostic Output Failure
1
1
Mechanical Jam
1
1
No Flow
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
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
151
151
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
No Patient Involvement
12
12
Sepsis
12
12
Obstruction/Occlusion
10
10
No Information
10
10
Insufficient Information
10
10
Renal Failure
8
8
Tissue Damage
6
6
Urinary Tract Infection
6
6
Perforation
6
6
Septic Shock
5
5
Pain
4
4
Hematuria
4
4
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
4
4
Device Embedded In Tissue or Plaque
4
4
Blood Loss
3
3
Pseudoaneurysm
3
3
Unspecified Infection
3
3
Abscess
3
3
Fistula
2
2
Hematoma
2
2
Pleural Effusion
2
2
Pneumonia
2
2
Pneumothorax
2
2
Post Operative Wound Infection
2
2
Respiratory Failure
2
2
Failure of Implant
2
2
Internal Organ Perforation
2
2
Transient Ischemic Attack
1
1
Urinary Retention
1
1
Perforation of Vessels
1
1
Anxiety
1
1
Liver Damage/Dysfunction
1
1
Hemothorax
1
1
Hypovolemic Shock
1
1
Pulmonary Embolism
1
1
Abdominal Pain
1
1
Cardiac Arrest
1
1
Deposits
1
1
Purulent Discharge
1
1
Embolism
1
1
Fever
1
1
Bowel Perforation
1
1
Fluid Discharge
1
1
Respiratory Insufficiency
1
1
Unspecified Kidney or Urinary Problem
1
1
Unspecified Tissue Injury
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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