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TPLC
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show TPLC since
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Device
cutter, wire
Product Code
HXZ
Regulation Number
888.4540
Device Class
1
MDR Year
MDR Reports
MDR Events
2019
36
36
2020
24
24
2021
44
44
2022
37
37
2023
33
33
2024
29
29
Device Problems
MDRs with this Device Problem
Events in those MDRs
Break
110
110
Material Integrity Problem
32
32
Failure to Cut
13
13
Fracture
13
13
Dull, Blunt
10
10
Material Deformation
7
7
Mechanical Problem
5
5
Crack
3
3
Contamination /Decontamination Problem
3
3
Material Fragmentation
3
3
Naturally Worn
3
3
Device Slipped
2
2
Activation, Positioning or Separation Problem
2
2
Adverse Event Without Identified Device or Use Problem
2
2
Detachment of Device or Device Component
2
2
Material Frayed
1
1
Device-Device Incompatibility
1
1
Compatibility Problem
1
1
Physical Resistance/Sticking
1
1
Device Fell
1
1
Defective Device
1
1
Component Missing
1
1
Material Twisted/Bent
1
1
Packaging Problem
1
1
No Apparent Adverse Event
1
1
Difficult to Open or Close
1
1
Corroded
1
1
Flaked
1
1
Mechanical Jam
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
129
129
No Consequences Or Impact To Patient
28
28
No Patient Involvement
15
15
Insufficient Information
10
10
No Known Impact Or Consequence To Patient
9
9
Foreign Body In Patient
6
6
No Information
3
3
No Code Available
3
3
Device Embedded In Tissue or Plaque
1
1
Hemorrhage/Bleeding
1
1
Laceration(s)
1
1
Tissue Damage
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Zimmer Biomet, Inc.
II
Dec-22-2020
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