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A new approval for smallest defibrillation lead of its kind | Post-TAVR bleeding | Key details about reprocessed catheter recall

News You Need to Know Today
A new approval for smallest defibrillation lead of its kind | Post-TAVR bleeding | Key details about reprocessed catheter recall
Friday, April 10, 2026
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Editor's Choice: Heart Rhythm

FDA approves smallest defibrillation lead of its kind for LBBA placement

The OmniaSecure defibrillation lead from Medtronic is already approved for placement in the right ventricle. This latest approval covers the left bundle branch area, opening the door for conduction system pacing and other advanced techniques.

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OmniaSecure defibrillation lead approved by FDA for placement in LBB area
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FDA approves smallest defibrillation lead of its kind for LBBA placement

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OmniaSecure defibrillation lead approved by FDA for placement in LBB area
The OmniaSecure defibrillation lead from Medtronic is already approved for placement in the right ventricle. This latest approval covers the left bundle branch area, opening the door for conduction system pacing and other advanced techniques.
READ MORE >

Post-TAVR bleeding in AFib patients much less common with apixaban than rivaroxaban

When it came to all-cause mortality and ischemic stroke, however, the two popular DOACs were associated with comparable outcomes. 

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IVUS guidance during DES implantation boosts long-term outcomes in new study
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Post-TAVR bleeding in AFib patients much less common with apixaban than rivaroxaban

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IVUS guidance during DES implantation boosts long-term outcomes in new study
When it came to all-cause mortality and ischemic stroke, however, the two popular DOACs were associated with comparable outcomes. 
READ MORE >

FDA shares details about reprocessed catheter recall

Back in February, the FDA expanded a recall of several reprocessed EP and ultrasound catheters due to a risk of contamination. The agency is now sharing additional information with the public.

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FDA issues recall of imaging systems
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FDA shares details about reprocessed catheter recall

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FDA issues recall of imaging systems
Back in February, the FDA expanded a recall of several reprocessed EP and ultrasound catheters due to a risk of contamination. The agency is now sharing additional information with the public.
READ MORE >

Cardiologist makes history with first commercial implant of new pacing lead for LBBAP

The first FDA-approved pacing lead specifically developed for LBBAP is now being implanted throughout the United States. 

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Xiaodong Zhang, MD, PhD,
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Cardiologist makes history with first commercial implant of new pacing lead for LBBAP

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Xiaodong Zhang, MD, PhD,
The first FDA-approved pacing lead specifically developed for LBBAP is now being implanted throughout the United States. 
READ MORE >

Johnson & Johnson launches faster PFA system in Europe

The new version of the PFA system is five times faster than the current catheter to improve workflow.

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Johnson & Johnson announced the launch of its new Varipulse Pro pulsed field ablation (PFA) system in Europe following CE mark approval. It is five times faster at ablation delivery at a cooler temperature than the previous version.
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Johnson & Johnson launches faster PFA system in Europe

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Johnson & Johnson announced the launch of its new Varipulse Pro pulsed field ablation (PFA) system in Europe following CE mark approval. It is five times faster at ablation delivery at a cooler temperature than the previous version.
The new version of the PFA system is five times faster than the current catheter to improve workflow.
READ MORE >

First patients treated in new PFA trial

The new nPulse nanosecond pulsed field ablation system uses five‑second applications to create lesions. It does not require catheter repositioning.

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Pulse Biosciences nPulse nanosecond pulsed field ablation (nsPFA) system uses 5‑second applications to create lesions and does not require catheter repositioning.
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First patients treated in new PFA trial

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Pulse Biosciences nPulse nanosecond pulsed field ablation (nsPFA) system uses 5‑second applications to create lesions and does not require catheter repositioning.
The new nPulse nanosecond pulsed field ablation system uses five‑second applications to create lesions. It does not require catheter repositioning.
READ MORE >

In Case You Missed It

Gore completes acquisition of medtech company behind next-gen heart device

Gore has officially acquired Conformal Medical, the company known for an investigational LAAO device that uses a proprietary foam implant. The transaction was first announced in January.

READ MORE >
Conformal Medical CLAAS
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Gore completes acquisition of medtech company behind next-gen heart device

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Conformal Medical CLAAS
Gore has officially acquired Conformal Medical, the company known for an investigational LAAO device that uses a proprietary foam implant. The transaction was first announced in January.
READ MORE >

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