Safety Alert Resource Center

FDA Warning Letter to Abbott (St Jude Medical Inc.)- (04/17/2017_- On April 12th, 2017 the U.S. Food and Drug Administration (FDA) issued notification to Abbott (St Jude Medical Inc.) that they were in violation of 4 codes of federal regulations (CFRs).  This notification was part of the enforcement phase of the FDA’s ongoing investigation of issues with Abbott’s (St Jude Medical Inc.) ICD pulse generators and transmitters. Learn more

St. Jude Merlin@home Transmitter (01/09/2017) - On January 9, 2017 the US Food and Drug Administration (FDA) and the Department of Homeland Security (DHS) issued a safety communication regarding a cybersecurity vulnerability of the St. Jude Merlin@home Transmitter. Learn more

Premature Battery Depletion of St. Jude Medical ICD and CRT-D Devices (10/11/2016)- On October 11 2016, the U.S. Food and Drug Administration issued a safety communication alerting health care providers and patients about premature battery depletion in a subset of St. Jude Medical ICD and CRT-D devices. Learn more