Medtronic Recalls Ventricular Assist Device Batteries
Medtronic is recalling HeartWare Ventricular Assist Device System batteries due to their ability to experience electrical faults that cause them to unexpectedly fail.
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Integra Pulls Intracranial Pressure Monitors for Inaccurate Readings
Integra LifeSciences initiated the global product removal of pressure monitor devices following consultation with the U.S. FDA.
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Medtronic Recalls Defibrillator Devices for Short Circuit Alert Risks
Medtronic is recalling Cobalt/Crome implantable cardioverter defibrillators and cardiac resynchronization therapy defibrillators.
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Medical Device Recalls Hit Two-Year High in Q2, Report Finds
The number of medical device recalls hit a two-year high in Q2 2022, data from Sedgwick’s Recall Index 2022 Edition 2 shows.
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Philips Recall Sparks 48K Complaints to FDA in Three Months, Including 44 Deaths
The FDA updated a safety communication regarding the ongoing recall issues of Philips’ respiratory devices.
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