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Cobalt XT HF CRT-D MRI SureScan Adverse Events: FDA MAUDE Data

MEDTRONIC, INC. · CRT-Defibrillator (CRT-D) · First cleared Apr 2020

Total Reports

513

Reports (30d)

15

Active Signals

1

Open Recalls

78

Monthly Report Volume

Event Type Breakdown

What the reports describe · Claripulse analysis

Most commonly reported problems

1

CRT Device Explanted Due to Infection

cardiac resynchronization, crt, infection, patient complications, result event

21

reports

2

Inappropriate Therapy for Tachycardia

crt, atrial, therapy, tachycardia, ventricular tachycardia

14

reports

3

Left Ventricular Lead Not Capturing

lead explanted, replaced, left ventricular, ventricular lead, capture

3

reports

4

Set Screw Failure During CRT Implant

resynchronization, defibrillator crt, crt, resynchronization therapy, therapy defibrillator

3

reports

5

Difficulty Interrogating CRT Device

resynchronization, defibrillator crt, crt, resynchronization therapy, therapy defibrillator

3

reports

6

Oversensing from Electromagnetic Interference

defibrillator crt, resynchronization, cardiac resynchronization, crt, resynchronization therapy

2

reports

Problem groupings are generated by Claripulse from report narrative text. They summarize what reporters wrote, not adjudicated root cause.

Detection

Active safety signals

Disproportionate reportinghigh

Regulatory

FDA recalls for this device

Class II

Apr 16, 2024 · Open, Classified

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

Class II

Apr 16, 2024 · Open, Classified

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

Class II

Apr 16, 2024 · Open, Classified

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

Class II

Apr 16, 2024 · Open, Classified

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

Class II

Apr 16, 2024 · Open, Classified

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

Class II

Apr 16, 2024 · Open, Classified

Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.

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Understanding this data

What FDA MAUDE data does and does not tell you

How these reports are filed, why raw counts mislead, and the limits to know before drawing conclusions.

How a safety signal is detected

What the "Active Signals" count above means and the methods that separate a real signal from noise.

Disclaimer: This system analyzes publicly available FDA MAUDE data. It does NOT provide medical advice. MAUDE data is de-identified. Do not attempt re-identification. Report counts may differ from the FDA's MAUDE search due to processing cadence and deduplication. Data is updated weekly.