St.Jude Medical Riata And Riata St Silicone Endocardial Defibrillation Leads

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St. Jude Medical Riata and Riata ST Silicone Endocardial …

https://www.cardiovascular.abbott/content/dam/bss/divisionalsites/cv/pdf/riata/Important_Product_Information_Riata_Silicone_Leads.PDF

Optim insulation, St. Jude Medical is completing the planned phase-out of all models of Riata and Riata ST silicone leads by December 31, 2010. If you are following …

Class 1 Device Recall Riata ST Silicone Insulated Leads

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=105847

For Additional Information Contact. 818-362-6822. Manufacturer Reason. for Recall. The recall was initiated because St. Jude Medical has confirmed the failures …

Riata Defibrillation Leads Communications | Abbott

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

Specifically, St. Jude Medical, in consultation with our independent leads Medical Advisory Board (MAB), voluntarily communicated proactively to physicians and …

MEDICAL DEVICE ADVISORY IMPORTANT …

https://www.cardiovascular.abbott/content/dam/bss/divisionalsites/cv/pdf/riata/Nov_2011_Important_Product_Information_Update_Riata_112811.pdf

St. Jude Medical Cardiac Rhythm Management Division 15900 Valley View Court Sylmar, CA 91342-3577 USA Tel 818 362 6822 800 423 5611 www.sjm.com . November 28, 2011 …

St. Jude Medical, Riata and Riata ST Silicone Endocardial ...

https://www.eeworldonline.com/st-jude-medical-riata-and-riata-st-silicone-endocardial-defibrillation-leads-class-1-recall-failures-with-lead-insulation/

AUDIENCE: Cardiology, Emergency Medicine, Risk Manager ISSUE: FDA notified healthcare professionals of a Class I Recall of the St. Jude Medical Riata and Riata ST …

FDA Calls Class 1 Recall For Riata, Riata ST …

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

December 16, 2011 – St. Jude Medical began a voluntary recall Nov. 28 for its Riata and Riata ST Silicone Defibrillation Leads, which the U.S. Food and Drug …

Class 1 Device Recall Riata - Food and Drug Administration

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

Sylmar CA 91342-3577. For Additional Information Contact. 818-362-6822. Manufacturer Reason. for Recall. St. Jude Medical has confirmed the failures associated …

IMPORTANT PRODUCT INFORMATION UPDATE - Abbott

https://www.cardiovascular.abbott/content/dam/bss/divisionalsites/nm/pdfs/int/riata/DOC2Important_Product_Information_Update_Riata_Riata_ST_Externalized.pdf

failure on our Riata® (8Fr) and Riata ST (7Fr) silicone endocardial defibrillation leads, with a specific emphasis on externalized conductors. The information provided is based …

Notice to Hospitals - Health Canada Endorsed Important …

https://www.cardiovascular.abbott/content/dam/bss/divisionalsites/nm/pdfs/int/riata/NTH_Riata_Final_HC_Approved_EN_POST_20121031.pdf

St. Jude Medical Riata and Riata ST Silicone Endocardial Defibrillation Leads October 31, 2012 Dear Health Professional, Please distribute to the relevant …

Recall: St. Jude Medical Riata and Raiata ST silicone endocardial ...

https://sweeneylawfirm.com/blog/medical-malpractice/recall-st-jude-medical-riata-and-raiata-st-silicone-endocardial-defibrillator-leads

Approximately 79,000 patients have implantable cardioverter defibrillator leads manufactured by St. Jude Medical are part of a class 1 recall because of electrical …

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