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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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New Search show TPLC since Back to Search Results
Device joint, knee, external brace
Product CodeITQ
Regulation Number 890.3475
Device Class 1

MDR Year MDR Reports MDR Events
2014 7 7
2015 6 6
2016 16 16
2017 8 8
2018 12 12
2019 76 76
2020 22 22
2021 4 4
2022 5 5
2023 75 75
2024 47 47

Device Problems MDRs with this Device Problem Events in those MDRs
Mechanical Problem 119 119
Unintended System Motion 118 118
Adverse Event Without Identified Device or Use Problem 95 95
No Apparent Adverse Event 24 24
Patient Device Interaction Problem 9 9
Insufficient Information 7 7
Break 7 7
Patient-Device Incompatibility 5 5
Device Operates Differently Than Expected 5 5
Detachment of Device or Device Component 3 3
Material Twisted/Bent 2 2
Use of Device Problem 2 2
Mechanical Jam 2 2
Inadequacy of Device Shape and/or Size 2 2
Collapse 2 2
Defective Component 2 2
Defective Device 2 2
Fracture 2 2
Physical Resistance/Sticking 2 2
Detachment Of Device Component 1 1
Deformation Due to Compressive Stress 1 1
Loose or Intermittent Connection 1 1
Unexpected Therapeutic Results 1 1
Human-Device Interface Problem 1 1
Missing Value Reason 1 1
Labelling, Instructions for Use or Training Problem 1 1
Material Deformation 1 1
Off-Label Use 1 1
Migration or Expulsion of Device 1 1
Component Incompatible 1 1
Appropriate Term/Code Not Available 1 1
Material Integrity Problem 1 1
Unintended Movement 1 1
Device Fell 1 1
Crack 1 1
Unstable 1 1
Device Slipped 1 1
Folded 1 1
Failure to Align 1 1
Device Packaging Compromised 1 1
Component Missing 1 1
Misassembled During Installation 1 1
Contamination /Decontamination Problem 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 119 119
Damage to Ligament(s) 68 68
Fall 13 13
Injury 13 13
Bone Fracture(s) 8 8
Pain 8 8
No Consequences Or Impact To Patient 6 6
Tissue Damage 5 5
Laceration(s) 5 5
No Known Impact Or Consequence To Patient 4 4
Patient Problem/Medical Problem 3 3
Joint Dislocation 3 3
Abrasion 3 3
Insufficient Information 3 3
Swelling 3 3
Unspecified Infection 2 2
Bruise/Contusion 2 2
Complaint, Ill-Defined 2 2
Hematoma 2 2
Rash 2 2
Ambulation Difficulties 1 1
Tissue Breakdown 1 1
Lead(s), Burn(s) From 1 1
Skin Tears 1 1
Swelling/ Edema 1 1
Unspecified Tissue Injury 1 1
Limb Fracture 1 1
Fluid Discharge 1 1
Peroneal Nerve Palsy 1 1
Thrombosis 1 1
Discomfort 1 1
Cramp(s) 1 1
Loss of Range of Motion 1 1
Thrombosis/Thrombus 1 1
Convulsion, Tonic 1 1
Skin Erosion 1 1
Cellulitis 1 1
Blister 1 1
Edema 1 1
Blood Loss 1 1
Rupture 1 1
Scarring 1 1
Inflammation 1 1
Sprain 1 1
Necrosis 1 1
Fungal Infection 1 1
Skin Irritation 1 1
Hip Fracture 1 1
Hypersensitivity/Allergic reaction 1 1
Convulsion, Clonic 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Corflex II Jan-04-2016
2 DeRoyal Industries Inc II Dec-19-2019
3 Mueller Sports Medicine, Inc II Jun-30-2020
4 Ossur H / F II Mar-31-2016
5 United Surgical Associates II May-23-2015
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