Riata Medical Device

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Riata Defibrillation Leads Communications | Abbott

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

We voluntarily and proactively stopped selling our Riata™ and Riata ST Silicone Defibrillation Leads in December 2010. We have communicated to physicians …

MEDICAL DEVICE ADVISORY IMPORTANT PRODUCT …

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

Riata ST silicone leads, St. Jude Medical and the MAB make the following recommendations, which are consistent with standard best practices and our December …

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 …

Here We Go Again — Another Failure of …

https://www.nejm.org/doi/full/10.1056/NEJMp1114695

U.S. patients continue to be exposed to underperforming and potentially hazardous medical …

Riata and Riata ST Silicone cardiac leads - increased wear

https://www.tga.gov.au/news/safety-alerts/riata-and-riata-st-silicone-cardiac-leads-increased-wear

26 November 2013. St Jude Medical has released updated data about Riata and Riata ST silicone cardiac leads. The November 2013 edition of the TGA's Medical Devices Safety …

The Riata Recall

https://www.hmpgloballearningnetwork.com/site/eplab/articles/riata-recall

The Riata lead has a failure mechanism that differs from other defibrillator leads. The conductor cables can erode through their silicone insulation channel from the inside out …

Class 1 Device Recall Riata ST Silicone Insulated Leads

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

St. Jude Medical Riata ST Silicone Endocardial Defibrillation Leads Riata(7Fr), Models: 7000, 7001, 7002, 7010, 7011, 7040, 7041, 7042 Product Usage: …

FDA Calls Class 1 Recall For Riata, Riata ST …

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

FDA Calls Class 1 Recall For Riata, Riata ST Defibrillation Leads. December 16, 2011 – St. Jude Medical began a voluntary recall Nov. 28 for its Riata and …

Medtronic confirms Hauser's findings - MassDevice

https://www.massdevice.com/medtronic-confirms-hausers-riata-findings/

The device maker demanded a retraction of the study, which culled 133 lead-related deaths from the FDA’s MAUDE database and linked 22 to problems with the Riata leads. …

Medical Device OPTIM RIATA ST MODEL 7020 - 7020/XX

https://www.medicaldevices24.com/medical_devices/info/optim-riata-st-model-7020/2236

The medical device OPTIM RIATA ST MODEL 7020 is realized by ST. JUDE MEDICAL INC. Della stessa categoria di dispositivi medici: RIATA ST MODEL 7021 OPTIM - …

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