St.Jude Medical Lead Advisory

Cardiovascular Product Advisories | Abbott

https://www.cardiovascular.abbott/us/en/hcp/product-advisories.html

St. Jude Medical Field Sales Staff and Field Clinical Engineers will install this software upgrade in Merlin PCS and Model 3510 programmers in the field. Thereafter, upon initial interrogation of an Epic …

St. Jude Medical issues advisory on Optisure leads

https://www.startribune.com/st-jude-medical-issues-advisory-on-optisure-leads/366273131/

In 2011, St. Jude Medical recalled 227,000 Riata or Riata ST model defibrillation leads because of premature erosion of wire insulation. The company agreed …

St. Jude's Durata lead is facing new questions - Star …

https://www.startribune.com/st-jude-s-durata-lead-is-facing-new-questions/210107621/

A report involving a failed Durata defibrillator lead has been published in an online journal, renewing concerns that St. Jude Medical’s newest device that connects a …

Abbott (formally known as “St. Jude Medical”) Recalls …

https://www.fda.gov/medical-devices/medical-device-recalls/abbott-formally-known-st-jude-medical-recalls-assuritytm-and-enduritytm-pacemakers-potential

Advisory Boards - St. Jude Children's Research Hospital

https://www.stjude.org/about-st-jude/leadership/advisory-boards.html

The Scientific Advisory Board is an autonomous panel of renowned physicians and scientists who help foster the medical and scientific development of St. Jude, providing guidance and insight on research …

Riata Defibrillation Leads Communications | Abbott

https://www.cardiovascular.abbott/us/en/hcp/product-advisories/riata.html

The main findings include: 1) the prevalence of externalized conductors (EC) and electrical dysfunction (ED) was highest in Riata and Riata ST leads; 2) the risk of …

FDA Calls Class 1 Recall For Riata, Riata ST …

https://www.dicardiology.com/content/fda-calls-class-1-recall-riata-riata-st-defibrillation-leads

Changes in impedance from three high voltage lead vectors (RVC to Can, SVC to Can, and RVC to SVC), as well as pacing and sensing electrodes, can be …

Class 1 Device Recall Riata - Food and Drug Administration

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=105844

St. Jude Medical Riata (8Fr), Models: 1560, 1561, 1562, 1570, 1571, 1572, 1580, 1581, 1582, 1590, 1591, 1592 Product Usage: These Silicone transvenous high …

Class 2 Device Recall QuickFlex, QuickFlex XL

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=108651

Doctors with any questions or concerns are instructed to contact their local St. Jude Medical representative or their Technical Services Department at (800) 722-3774. …

St. Jude Durata Lead Issues | Durata Lead Failure

https://www.classaction.org/durata-leads

Injured by a St. Jude Durata Lead? If you or a loved one has been injured by a St. Jude Durata defibrillator lead, you may be able to file a claim seeking …