The rate of confirmed cases of the “externalized conductor” phenomenon with St. Jude Medical’s no-longer-marketed, silicone-insulated Riata implantable defibrillator lead climbed to 0.3% as of Feb. 29, according to the firm’s latest cardiac rhythm management product performance report, released May 1.
The rate was 0.17% as of Dec. 31 and 0.1% of last November, when St. Jude issued an advisory for the products that was categorized as a class I recall...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Medtech Insight for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?