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TPLC
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show TPLC since
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Device
driver, prosthesis
Product Code
HWR
Regulation Number
888.4540
Device Class
1
MDR Year
MDR Reports
MDR Events
2014
2
2
2015
191
191
2016
436
436
2017
707
707
2018
574
574
2019
678
678
2020
738
738
2021
898
898
2022
980
980
2023
1281
1281
2024
454
454
Device Problems
MDRs with this Device Problem
Events in those MDRs
Break
3594
3594
Material Twisted/Bent
1349
1349
Material Deformation
646
646
Device-Device Incompatibility
637
637
Naturally Worn
362
362
Crack
269
269
Fracture
185
185
Appropriate Term/Code Not Available
107
107
Entrapment of Device
98
98
Device Slipped
85
85
Mechanical Jam
80
80
Mechanical Problem
72
72
Material Integrity Problem
69
69
Component Missing
49
49
Contamination /Decontamination Problem
40
40
Scratched Material
34
34
Physical Resistance/Sticking
28
28
Adverse Event Without Identified Device or Use Problem
27
27
Unintended Movement
24
24
Connection Problem
23
23
Detachment of Device or Device Component
18
18
Bent
17
17
Material Split, Cut or Torn
17
17
Material Fragmentation
12
12
Difficult to Remove
12
12
Calibration Problem
12
12
Structural Problem
12
12
No Apparent Adverse Event
12
12
Insufficient Information
12
12
Use of Device Problem
11
11
Corroded
10
10
Torn Material
9
9
Difficult to Insert
7
7
Loose or Intermittent Connection
7
7
Detachment Of Device Component
6
6
Failure to Cut
6
6
Device Contamination with Chemical or Other Material
5
5
Material Torqued
5
5
Separation Failure
4
4
Device Operates Differently Than Expected
4
4
Defective Device
4
4
Device Issue
4
4
Improper or Incorrect Procedure or Method
4
4
Disassembly
3
3
Material Discolored
3
3
Dull, Blunt
3
3
Defective Component
3
3
Failure to Disconnect
3
3
Output Problem
3
3
Separation Problem
3
3
Illegible Information
3
3
Device Handling Problem
2
2
Material Distortion
2
2
Flaked
2
2
Fitting Problem
2
2
Sticking
2
2
Misconnection
2
2
Delivered as Unsterile Product
1
1
Output above Specifications
1
1
Peeled/Delaminated
1
1
Off-Label Use
1
1
Material Separation
1
1
Migration or Expulsion of Device
1
1
Device Inoperable
1
1
Incomplete or Missing Packaging
1
1
Residue After Decontamination
1
1
Device Damaged Prior to Use
1
1
Disconnection
1
1
Component Incompatible
1
1
Thermal Decomposition of Device
1
1
Device Reprocessing Problem
1
1
Packaging Problem
1
1
Moisture or Humidity Problem
1
1
Device Difficult to Maintain
1
1
Failure to Align
1
1
Compatibility Problem
1
1
Migration
1
1
Device Fell
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
3504
3504
No Consequences Or Impact To Patient
1732
1732
No Known Impact Or Consequence To Patient
753
753
No Information
501
501
Insufficient Information
226
226
Not Applicable
125
125
No Code Available
103
103
Foreign Body In Patient
73
73
Device Embedded In Tissue or Plaque
42
42
No Patient Involvement
41
41
Injury
17
17
Spinal Column Injury
4
4
Bone Fracture(s)
4
4
Limb Fracture
4
4
Local Reaction
3
3
Blood Loss
2
2
Hip Fracture
2
2
Failure of Implant
2
2
Foreign Body Reaction
2
2
Pain
2
2
Burn(s)
1
1
Death
1
1
Nerve Damage
1
1
Neuropathy
1
1
Internal Organ Perforation
1
1
Reaction
1
1
Spinal Cord Injury
1
1
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Biomet Microfixation, Inc.
II
Apr-11-2010
2
Biomet U.K., Ltd.
II
Feb-22-2017
3
Smith & Nephew, Inc., Endoscopy Div.
II
Jan-29-2016
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