SENZA

NEVRO SENZA

This device is manufactured by NEVRO CORP.

The following problems were reported about this device:

Year Description Events/year Type
2024 Wound Dehiscence 8 Patient
2024 Unspecified Kidney or Urinary Problem 1 Patient
2024 Unspecified Infection 111 Patient
2024 Unspecified Heart Problem 4 Patient
2024 Unspecified Gastrointestinal Problem 1 Patient
2024 Undesired Nerve Stimulation 2 Patient
2024 Ulcer 1 Patient
2024 Thrombosis/Thrombus 1 Patient
2024 Tachycardia 1 Patient
2024 Syncope/Fainting 2 Patient
2024 Swelling/ Edema 6 Patient
2024 Stroke/CVA 3 Patient
2024 Skin Erosion 3 Patient
2024 Seroma 4 Patient
2024 Sepsis 5 Patient
2024 Respiratory Failure 1 Patient
2024 Pulmonary Embolism 1 Patient
2024 Post Operative Wound Infection 2 Patient
2024 Pocket Erosion 3 Patient
2024 Pneumonia 1 Patient
2024 Paresthesia 3 Patient
2024 Paralysis 5 Patient
2024 Pain 17 Patient
2024 Numbness 6 Patient
2024 Nerve Damage 1 Patient
2024 Neck Stiffness 1 Patient
2024 Neck Pain 1 Patient
2024 Myocardial Infarction 4 Patient
2024 Muscle Weakness/Atrophy 1 Patient
2024 Meningitis 1 Patient
2024 Liver Failure 1 Patient
2024 Ischemic Heart Disease 2 Patient
2024 Intracranial Pressure Increased 1 Patient
2024 Insufficient Information 58 Patient
2024 Inadequate Pain Relief 2 Patient
2024 Implant Pain 36 Patient
2024 Impaired Healing 10 Patient
2024 Hypersensitivity/Allergic reaction 3 Patient
2024 Hernia 1 Patient
2024 Hemorrhagic Stroke 1 Patient
2024 Hemorrhage/Blood Loss/Bleeding 1 Patient
2024 Hematoma 7 Patient
2024 Heart Failure/Congestive Heart Failure 1 Patient
2024 Headache 3 Patient
2024 Gastrointestinal Hemorrhage 1 Patient
2024 Fungal Infection 1 Patient
2024 Fibrosis 1 Patient
2024 Fever 1 Patient
2024 Fall 3 Patient
2024 Encephalopathy 1 Patient
2024 Electric Shock 1 Patient
2024 Discomfort 6 Patient
2024 Dementia 3 Patient
2024 Cramp(s) /Muscle Spasm(s) 2 Patient
2024 Convulsion/Seizure 5 Patient
2024 Cerebrospinal Fluid Leakage 8 Patient
2024 Cellulitis 1 Patient
2024 Cardiomyopathy 1 Patient
2024 Cardiac Arrest 4 Patient
2024 Cancer 8 Patient
2024 Burning Sensation 6 Patient
2024 Bruise/Contusion 2 Patient
2024 Balance Problems 1 Patient
2024 Bacterial Infection 20 Patient
2024 Bacteremia 1 Patient
2024 Arteriosclerosis/ Atherosclerosis 1 Patient
2024 Appropriate Term / Code Not Available 1 Patient
2024 Ambulation Difficulties 4 Patient
2024 Abdominal Pain 2 Patient
2024 Use of Incorrect Control/Treatment Settings 1 Device
2024 Migration 1 Device
2024 Leak/Splash 1 Device
2024 Insufficient Information 22 Device
2024 Fracture 2 Device
2024 Failure to Charge 1 Device
2024 Detachment of Device or Device Component 3 Device
2024 Adverse Event Without Identified Device or Use Problem 259 Device
2023 Wound Dehiscence 4 Patient
2023 Vomiting 2 Patient
2023 Urinary Retention 1 Patient
2023 Unspecified Kidney or Urinary Problem 2 Patient
2023 Unspecified Infection 38 Patient
2023 Unspecified Heart Problem 5 Patient
2023 Unspecified Gastrointestinal Problem 1 Patient
2023 Syncope/Fainting 1 Patient
2023 Swelling/ Edema 2 Patient
2023 Stroke/CVA 4 Patient
2023 Speech Disorder 1 Patient
2023 Skin Erosion 2 Patient
2023 Skin Burning Sensation 2 Patient
2023 Shock from Patient Lead(s) 2 Patient
2023 Seroma 1 Patient
2023 Sepsis 2 Patient
2023 Respiratory Failure 1 Patient
2023 Renal Failure 3 Patient
2023 Reduced Blood Flow 1 Patient
2023 Pulmonary Embolism 3 Patient
2023 Post Operative Wound Infection 2 Patient
2023 Pneumothorax 1 Patient
2023 Pneumonia 2 Patient
2023 Paralysis 7 Patient
2023 Pain 15 Patient
2023 Osteomyelitis 1 Patient
2023 Obstruction/Occlusion 1 Patient
2023 Numbness 5 Patient
2023 Neuropathy 1 Patient
2023 Needle Stick/Puncture 1 Patient
2023 Neck Pain 1 Patient
2023 Myocardial Infarction 1 Patient
2023 Muscle Weakness/Atrophy 5 Patient
2023 Movement Disorder 1 Patient
2023 Low Oxygen Saturation 2 Patient
2023 Low Blood Pressure/ Hypotension 1 Patient
2023 Intervertebral Disc Compression or Protrusion 1 Patient
2023 Insufficient Information 43 Patient
2023 Inadequate Pain Relief 3 Patient
2023 Implant Pain 18 Patient
2023 Impaired Healing 7 Patient
2023 Hypersensitivity/Allergic reaction 3 Patient
2023 High Blood Pressure/ Hypertension 1 Patient
2023 Hematoma 8 Patient
2023 Heart Failure/Congestive Heart Failure 2 Patient
2023 Headache 1 Patient
2023 Granuloma 1 Patient
2023 Fungal Infection 1 Patient
2023 Foreign Body In Patient 1 Patient
2023 Fibrosis 1 Patient
2023 Fall 5 Patient
2023 Electric Shock 2 Patient
2023 Ear Pain 1 Patient
2023 Convulsion/Seizure 2 Patient
2023 Cognitive Changes 1 Patient
2023 Coagulation Disorder 1 Patient
2023 Chronic Obstructive Pulmonary Disease (COPD) 2 Patient
2023 Chest Pain 1 Patient
2023 Cerebrospinal Fluid Leakage 8 Patient
2023 Cardiac Arrest 1 Patient
2023 Cancer 5 Patient
2023 Burning Sensation 6 Patient
2023 Bacterial Infection 4 Patient
2023 Aspiration Pneumonitis 1 Patient
2023 Arrhythmia 1 Patient
2023 Appropriate Term / Code Not Available 1 Patient
2023 Aortic Valve Insufficiency/ Regurgitation 1 Patient
2023 Ambulation Difficulties 2 Patient
2023 Abdominal Pain 1 Patient
2023 Positioning Problem 1 Device
2023 Misconnection 1 Device
2023 Migration 4 Device
2023 Mechanical Jam 1 Device
2023 Material Split, Cut or Torn 1 Device
2023 Material Frayed 2 Device
2023 Insufficient Information 15 Device
2023 Fracture 1 Device
2023 Device Dislodged or Dislocated 1 Device
2023 Detachment of Device or Device Component 5 Device
2023 Battery Problem 1 Device
2023 Adverse Event Without Identified Device or Use Problem 185 Device
2022 Wound Dehiscence 1 Patient
2022 Unspecified Respiratory Problem 1 Patient
2022 Unspecified Kidney or Urinary Problem 1 Patient
2022 Unspecified Infection 3 Patient
2022 Skin Erosion 1 Patient
2022 Skin Burning Sensation 1 Patient
2022 Seroma 1 Patient
2022 Sepsis 1 Patient
2022 Respiratory Failure 1 Patient
2022 Paralysis 1 Patient
2022 Pain 4 Patient
2022 Numbness 1 Patient
2022 Nerve Damage 1 Patient
2022 Myocardial Infarction 2 Patient
2022 Insufficient Information 14 Patient
2022 Inadequate Pain Relief 1 Patient
2022 Implant Pain 8 Patient
2022 Impaired Healing 2 Patient
2022 Hematoma 1 Patient
2022 Foreign Body In Patient 1 Patient
2022 Fall 2 Patient
2022 Dizziness 1 Patient
2022 Convulsion/Seizure 1 Patient
2022 Cognitive Changes 1 Patient
2022 Bacterial Infection 1 Patient
2022 Material Split, Cut or Torn 2 Device
2022 Insufficient Information 8 Device
2022 Detachment of Device or Device Component 1 Device
2022 Adverse Event Without Identified Device or Use Problem 110 Device
2021 Unspecified Infection 1 Patient
2021 Stroke/CVA 1 Patient
2021 Multiple Organ Dysfunction Syndrome 1 Patient
2021 Insufficient Information 3 Patient
2021 Cognitive Changes 2 Patient
2021 Chest Pain 1 Patient
2021 Appropriate Term / Code Not Available 1 Patient
2021 Detachment of Device or Device Component 1 Device
2021 Adverse Event Without Identified Device or Use Problem 13 Device
2020 Unspecified Infection 1 Patient
2020 Pain 1 Patient
2020 Abdominal Pain 1 Patient
2020 Fracture 1 Device
2020 Adverse Event Without Identified Device or Use Problem 6 Device