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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device suture, absorbable, natural
Product CodeGAL
Regulation Number 878.4830
Device Class 2

MDR Year MDR Reports MDR Events
2019 229 229
2020 109 109
2021 120 120
2022 130 130
2023 121 121
2024 73 73

Device Problems MDRs with this Device Problem Events in those MDRs
Break 428 428
Material Separation 159 159
Adverse Event Without Identified Device or Use Problem 55 55
Material Frayed 43 43
Detachment of Device or Device Component 37 37
Appropriate Term/Code Not Available 21 21
Material Integrity Problem 18 18
Patient-Device Incompatibility 15 15
Defective Component 15 15
Component Misassembled 13 13
Material Twisted/Bent 11 11
Use of Device Problem 10 10
Unraveled Material 9 9
Packaging Problem 8 8
Device Markings/Labelling Problem 7 7
Fluid/Blood Leak 6 6
Product Quality Problem 5 5
Device Contaminated During Manufacture or Shipping 5 5
Material Split, Cut or Torn 5 5
Difficult to Open or Close 4 4
Device Slipped 4 4
Difficult to Remove 3 3
Component Missing 3 3
Contamination /Decontamination Problem 3 3
Migration 2 2
Unsealed Device Packaging 2 2
Component Incompatible 2 2
Positioning Failure 1 1
Entrapment of Device 1 1
Material Fragmentation 1 1
Loose or Intermittent Connection 1 1
Delivered as Unsterile Product 1 1
Insufficient Information 1 1
Device Fell 1 1
Missing Information 1 1
Activation, Positioning or Separation Problem 1 1
Manufacturing, Packaging or Shipping Problem 1 1
Material Deformation 1 1
Mechanics Altered 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 370 370
No Consequences Or Impact To Patient 245 245
Insufficient Information 28 28
Wound Dehiscence 24 24
Not Applicable 20 20
No Code Available 19 19
Hemorrhage/Bleeding 18 18
Unspecified Infection 17 17
Foreign Body In Patient 16 16
No Known Impact Or Consequence To Patient 13 13
Pain 12 12
No Patient Involvement 10 10
Swelling/ Edema 10 10
Post Operative Wound Infection 9 9
No Information 8 8
Unspecified Tissue Injury 8 8
Blood Loss 6 6
Hypersensitivity/Allergic reaction 6 6
Erythema 6 6
Foreign Body Reaction 5 5
Cyst(s) 5 5
Skin Irritation 5 5
Skin Inflammation 5 5
Incontinence 4 4
Unintended Radiation Exposure 4 4
Granuloma 4 4
Inflammation 4 4
Erosion 3 3
Abscess 3 3
Tissue Damage 3 3
Scar Tissue 3 3
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 3 3
Device Embedded In Tissue or Plaque 3 3
Radiation Exposure, Unintended 2 2
Prolapse 2 2
Impaired Healing 2 2
Numbness 2 2
Obstruction/Occlusion 2 2
Blister 2 2
Abnormal Vaginal Discharge 2 2
Sepsis 2 2
Hematoma 2 2
Fistula 2 2
Itching Sensation 1 1
Laceration(s) 1 1
Necrosis 1 1
Adhesion(s) 1 1
Anaphylactic Shock 1 1
Calcium Deposits/Calcification 1 1
Edema 1 1
Seroma 1 1
Swelling 1 1
Tachycardia 1 1
Weakness 1 1
Urinary Tract Infection 1 1
Scarring 1 1
Low Blood Pressure/ Hypotension 1 1
Paralysis 1 1
Local Reaction 1 1
Respiratory Distress 1 1
Skin Inflammation/ Irritation 1 1
Stenosis 1 1
Urticaria 1 1
Discomfort 1 1
Hematuria 1 1
Tissue Breakdown 1 1
Fluid Discharge 1 1

Recalls
Manufacturer Recall Class Date Posted
1 CP Medical Inc II Mar-19-2019
2 Covidien, LP II Apr-12-2023
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