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TPLC
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show TPLC since
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Device
intestinal stimulator
Product Code
LNQ
Device Class
Humanitarian Device Exemption
MDR Year
MDR Reports
MDR Events
2014
413
413
2015
300
300
2016
377
377
2017
438
438
2018
325
325
2019
258
258
2020
177
177
2021
188
188
2022
185
185
2023
165
165
2024
102
102
Device Problems
MDRs with this Device Problem
Events in those MDRs
Adverse Event Without Identified Device or Use Problem
769
769
Device Operates Differently Than Expected
554
554
Inappropriate/Inadequate Shock/Stimulation
427
427
Insufficient Information
281
281
Migration or Expulsion of Device
261
261
High impedance
200
200
Electromagnetic Compatibility Problem
158
158
Break
147
147
Battery Problem
134
134
Premature Discharge of Battery
108
108
Failure to Deliver Energy
99
99
Unstable
93
93
Low Battery
89
89
Impedance Problem
88
88
Electromagnetic Interference
70
70
Unintended Collision
70
70
Malposition of Device
64
64
Patient Device Interaction Problem
59
59
Energy Output Problem
54
54
Pocket Stimulation
44
44
Communication or Transmission Problem
41
41
Intermittent Continuity
40
40
Overheating of Device
39
39
Material Deformation
37
37
Failure to Interrogate
34
34
Positioning Problem
32
32
Therapy Delivered to Incorrect Body Area
29
29
Entrapment of Device
26
26
Device Or Device Fragments Location Unknown
26
26
Disconnection
25
25
Appropriate Term/Code Not Available
24
24
Device Displays Incorrect Message
20
20
Connection Problem
15
15
Low impedance
15
15
Human-Device Interface Problem
13
13
Environmental Compatibility Problem
13
13
Shipping Damage or Problem
11
11
Device Contamination with Chemical or Other Material
11
11
Shelf Life Exceeded
10
10
Degraded
10
10
Unexpected Therapeutic Results
9
9
Material Erosion
8
8
Energy Output To Patient Tissue Incorrect
7
7
Vibration
6
6
Noise, Audible
6
6
Patient-Device Incompatibility
5
5
Device Dislodged or Dislocated
5
5
No Device Output
5
5
Electro-Static Discharge
5
5
Display or Visual Feedback Problem
5
5
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Known Impact Or Consequence To Patient
508
508
Pain
477
477
Vomiting
468
468
Nausea
444
444
Electric Shock
426
426
Complaint, Ill-Defined
401
401
Therapeutic Response, Decreased
391
391
Therapeutic Effects, Unexpected
323
323
No Clinical Signs, Symptoms or Conditions
197
197
Unspecified Infection
184
184
Abdominal Pain
178
178
Insufficient Information
157
157
Malaise
146
146
Discomfort
143
143
Paresis
138
138
Weight Changes
98
98
Undesired Nerve Stimulation
72
72
Erosion
68
68
No Code Available
64
64
Burning Sensation
63
63
Internal Organ Perforation
56
56
Constipation
54
54
Abdominal Distention
44
44
Obstruction/Occlusion
44
44
Failure of Implant
43
43
Swelling
41
41
Seroma
41
41
Diarrhea
40
40
Hernia
39
39
Muscle Spasm(s)
36
36
Pocket Erosion
35
35
Dehydration
29
29
Staphylococcus Aureus
25
25
Hemorrhage/Bleeding
24
24
Scar Tissue
24
24
Fever
22
22
Sepsis
21
21
Sleep Dysfunction
21
21
Abdominal Cramps
20
20
Test Result
20
20
Wound Dehiscence
19
19
Erythema
19
19
Bacterial Infection
19
19
Foreign Body In Patient
18
18
Twitching
18
18
Ambulation Difficulties
18
18
Urinary Tract Infection
18
18
Adhesion(s)
18
18
Twiddlers Syndrome
18
18
Headache
17
17
Recalls
Manufacturer
Recall Class
Date Posted
1
Medtronic Neuromodulation
II
Oct-29-2009
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