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This system analyzes publicly available FDA MAUDE data. It does NOT provide medical advice. MAUDE data is de-identified — do not attempt re-identification. © 2026 Claripulse.

Back to Cardiac Rhythm Management
MAUDE LookupCardiac Rhythm ManagementRESONATE HF ICD DR

RESONATE HF ICD DR Adverse Events: FDA MAUDE Data

BOSTON SCIENTIFIC CORPORATION · Implantable Cardioverter Defibrillator (ICD) · First cleared Jul 1997

Total Reports

423

Reports (30d)

21

Active Signals

1

Open Recalls

12

Monthly Report Volume
Event Type Breakdown

What the reports describe · Claripulse analysis

Most commonly reported problems

1

ICD Delivered Inappropriate ATP and Shocks

tachycardia pacing, tachycardia, delivered, anti tachycardia, atp

19

reports

2

ICD Explanted Due to Revision Infection

adverse, reported icd, effects, icd explanted, revision infection

13

reports

3

ICD Exhibited Oversensing Due to EMI

atrial, remains service, effects, oversensing, technical

8

reports

4

ICD Exhibited Undersensing During VT

atrial, undersensing, remains service, effects, icd exhibited

5

reports

5

ICD Exhibited High Shock Impedance Measurements

impedance measurements, measurements, effects, shock impedance, range

4

reports

6

ICD Unable to be Interrogated

adverse, remains service, effects, troubleshooting, service adverse

3

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 I

Aug 20, 2025 · Open, Classified

Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps).

Class I

Jul 24, 2025 · Open, Classified

Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early lead replacement. Most serious harm is death or need for cardiac resuscitation.

Class II

Nov 30, 2023 · Open, Classified

The software application on the Programmer/Recorder/Monitor (PRM) for Implantable Pulse Generators will display certain diagnostic dates incorrectly, with a year in the 1990s.

Class II

Jul 11, 2023 · Open, Classified

There is a potential for a rare interaction between the EMBLEM S-ICD and LATITUDE communicator, which may cause S-ICD sensing disablement for a 24-hour interval.

Class II

Jul 11, 2023 · Open, Classified

There is a potential for a rare interaction between the EMBLEM S-ICD and LATITUDE communicator, which may cause S-ICD sensing disablement for a 24-hour interval.

Class II

Feb 2, 2023 · Open, Classified

Under specific circumstances, the U.S. product registration system did not send up enablement requests to U.S. LATITUDE Customer Support during an 8-month interval in 2022. For these patients, the HeartLogic Index and any associated Yellow Alerts are currently not visible in LATITUDE as may have been intended by the healthcare provider..

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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.

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How a safety signal is detected

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

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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.