Source link : https://www.newshealth.biz/health-news/varipulse-heart-device-procedures-paused-after-safety-events/
Just months after FDA approval, Johnson & Johnson paused the rollout of its Varipulse pulsed field ablation (PFA) platform in the U.S. due to safety reasons. In a U.S. external evaluation cohort, four reported neurovascular events occurred among over 130 cases across 14 sites and 40 operators. “We are working diligently to complete the investigation […]
Author : News Health
Publish date : 2025-01-08 21:33:07
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