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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 …
The Riata Recall
- https://www.hmpgloballearningnetwork.com/site/eplab/articles/riata-recall
- Riata (8 French) Silicone Endocardial Defibrillation Leads (Models 1560, 1561, 1562, 1570, 1571, 1572, 1580, 1581, 1582, 1590, 1591, and 1592), and Riata ST (7 French) Silicone …
Performance of the St. Jude Medical Riata leads - PubMed
- https://pubmed.ncbi.nlm.nih.gov/19103512/
- During more than 22 months of follow-up of over 7,000 Riata leads in 4 prospective registries and clinical trials, the incidence of lead-related adverse events including …
Performance of the St. Jude Medical Riata Leads
- https://www.sciencedirect.com/science/article/pii/S1547527108010552
- Data from patients implanted with Riata ICD leads were obtained from 4 prospective studies: Advancements in ICD Therapy (ACT), OPTIM Lead InsUlation …
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: …
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 ...
Extraction of Recalled Riata Leads - innovationsincrm.com
- https://www.innovationsincrm.com/cardiac-rhythm-management/2013/july/475-extraction-of-recalled-riata-leads
- There are two types of recalled leads in the Riata family: the 8-French Riata model (released in 2002), and the 7-French Riata ST model (2005). Approximately 227,000 …
Performance of the St. Jude Medical Riata Leads
- https://www.heartrhythmjournal.com/article/S1547-5271(08)01055-2/abstract?code=hrthm-site
- Recent attention has been focused on the performance of high-voltage implantable cardioverter-defibrillator (ICD) leads. Lead-related adverse events can be caused by …
MAUDE Adverse Event Report: ST. JUDE MEDICAL …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/Detail.CFM?MDRFOI__ID=2747023&DEVICE_SEQUENCE_NO=2
- Model Number ST JUDE ICD VR RF: Device Problems Premature Discharge of Battery (1057); Nonstandard Device (1420) Patient Problem No Known Impact Or Consequence …
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