Topic Archives: St. Jude Riata Lead

St. Jude Riata Recall Sign of FDA Oversite Problems: Report

February 21, 2012 By: Staff Writers

A recent editorial published in the New England Journal of Medicine suggests that last year’s recall of St. Jude Riata defibrillator leads highlights ongoing problems with the FDA’s oversight of…
St. Jude Riata Defibrilator Lead Recall Issued Due to Risk of Failure

December 19, 2011 By: Staff Writers

Federal regulators have determined that a warning letter sent to doctors regarding problems with St. Jude Riata Silicone Defibrillation Leads constituted a Class I medical device recall.

Ozempic Intestinal Blockage Warnings Added to FDA Label About Gastrointestinal Risks (Posted 4 days ago)

The FDA is requiring new label warnings to alert patients and doctors to the risk of Ozempic intestinal blockage side effects.

Lawsuit Against Uber Alleges Rideshare Service Fails to Protect Customers From Sexual Assaults (Posted 5 days ago)

Eight women have filed Uber sexual assault lawsuits, claiming the rideshare service failed to protect them from predatory drivers due to its lack of safety measures.

Families Say Camp Lejeune Settlement Fails to Address Countless Miscarriages, Birth Defects Caused By Water Contamination (Posted 6 days ago)

A new report highlights how many women and families feel left out of Camp Lejeune settlement negotiations after suffering repeated miscarriages they say were caused by miscarriages on the North Carolina military base.

Topic Archives: St. Jude Riata Lead

St. Jude Riata Recall Sign of FDA Oversite Problems: Report

St. Jude Riata Defibrilator Lead Recall Issued Due to Risk of Failure

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