Friday, February 22, 2019

The lawsuits involving the St. Jude Implantable Cardioverter-Defibrillators (“ICD”) and Cardiac Resynchronization Therapy Devices (“CRT-D”) are being filed because the battery in the medical devices can fail without providing enough warning to patients that the battery needs replacing, and might not function when needed.

Below are the news stories and videos we have posted on this topic.

St. Jude Defibrillator News

FDA Issues Warning to Abbott Laboratories About Defective Devices

In a strongly-worded letter last week, the federal Food and Drug Administration issued a warning to medical device company Abbott Laboratories regarding defective heart defibrillators and a medical monitoring device with potential vulnerabilities to hackers.The issues are centered around three implantable defibrillators: the Fortify ICD, the Quadra Assura...