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 |