Medtronic Offers Hospitals Backup Controllers to Help Prevent HVAD Failures
Medtronic is suggesting health care professionals use mostly untested and unapproved software in backup controllers to help prevent HVAD restart failures.
Medtronic is suggesting health care professionals use mostly untested and unapproved software in backup controllers to help prevent HVAD restart failures.
Millions of consumers with recalled Philips CPAP machines have yet to receive replacement units, according to a new report.
The FDA warns of potentially fatal cybersecurity flaws linked to the Medtronic MiniMed 600 Series Insulin Pump System.
The FDA has updated a Medtronic breathing tubes recall to provide recommendations to healthcare professionals.
The Baxter Clearlink Basic Solution Sets recall comes after dozens of reports of leaks, which could expose patients and doctors to potentially toxic drug cocktails.
An investor lawsuit claims Medtronic hid MiniMed insulin pump problems from both the medical community and investors.
Following reports of patient deaths, nearly 400,000 Medtronic breathing tubes are being recalled due to the risk of airway obstruction.
The FDA warns that MitraClip heart valve repair devices may malfunction, resulting in a backflow of blood into the heart.
More than 23,000 Medtronic HVAD heart implants are being recalled due to reports of battery failures which have led to at least one patient death.
The FDA has announced a class I recall for thousands of BD needle kits and drivers used to access blood vessels in bones.