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TPLC
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Device
adaptor, hygiene
Regulation Description
Daily activity assist device.
Product Code
ILS
Regulation Number
890.5050
Device Class
1
MDR Year
MDR Reports
MDR Events
2020
32
33
2021
27
27
2022
45
45
2023
59
59
2024
37
37
2025
47
47
Device Problems
MDRs with this Device Problem
Events in those MDRs
Break
35
36
Material Integrity Problem
27
27
Collapse
24
24
Insufficient Information
22
22
Fracture
21
21
Material Twisted/Bent
17
17
Adverse Event Without Identified Device or Use Problem
14
14
Mechanical Problem
12
12
Appropriate Term/Code Not Available
12
12
Detachment of Device or Device Component
10
10
Unintended Movement
8
8
Material Fragmentation
6
6
Device Dislodged or Dislocated
6
6
Misassembly by Users
5
5
Material Separation
5
5
Loose or Intermittent Connection
5
5
Device Tipped Over
4
4
Use of Device Problem
4
4
Unstable
3
3
Crack
3
3
Structural Problem
3
3
Defective Component
2
2
Installation-Related Problem
2
2
Human-Device Interface Problem
2
2
Improper or Incorrect Procedure or Method
2
2
Device Slipped
1
1
Suction Failure
1
1
Material Puncture/Hole
1
1
Device Fell
1
1
Manufacturing, Packaging or Shipping Problem
1
1
Patient Device Interaction Problem
1
1
Component Missing
1
1
Sharp Edges
1
1
Solder Joint Fracture
1
1
Material Deformation
1
1
Product Quality Problem
1
1
No Apparent Adverse Event
1
1
Connection Problem
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
Fall
105
106
Head Injury
26
26
Bruise/Contusion
25
25
Insufficient Information
23
23
Bone Fracture(s)
21
21
Laceration(s)
20
20
Pain
17
17
No Clinical Signs, Symptoms or Conditions
16
16
Concussion
11
11
Limb Fracture
10
10
Swelling/ Edema
7
7
Vertebral Fracture
6
6
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available
6
6
Hip Fracture
4
4
Skin Tears
3
3
Muscle/Tendon Damage
3
3
Neck Pain
3
3
Abrasion
3
3
Muscle Weakness
3
3
Hematoma
3
3
Unspecified Infection
3
3
Easy Bruising
2
2
Multiple Fractures
2
2
Coma
2
2
Brain Injury
2
2
Intervertebral Disc Compression or Protrusion
2
2
Loss of consciousness
2
2
Tooth Fracture
1
1
Blister
1
1
Intracranial Hemorrhage
1
1
Needle Stick/Puncture
1
1
Loss of Range of Motion
1
1
Vertigo
1
1
Inflammation
1
1
Unspecified Musculoskeletal problem
1
1
Memory Loss/Impairment
1
1
Unspecified Kidney or Urinary Problem
1
1
Joint Dislocation
1
1
Skin Infection
1
1
Ulcer
1
1
Fracture, Arm
1
1
Unspecified Heart Problem
1
1
Hemorrhage/Bleeding
1
1
No Consequences Or Impact To Patient
1
1
Pressure Sores
1
1
Damage to Ligament(s)
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Gf Health Products
II
Apr-05-2021
2
James Leckey Design Ltd
II
Apr-08-2020
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