Getinge’s Recall of 11,000 Ventilators Labeled Class I Event by FDA
Getinge is recalling several different types of ventilators in its device portfolio that are being labeled as a Class I event by the FDA.
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Search Results for: recall
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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