HeartMate Devices Linked to Injuries and Deaths Receive FDA Recall

MIAMI, FL – The Food and Drug Administration has issued its most serious recall for two heart devices due to their connection to numerous injuries and deaths. The HeartMate 2 and HeartMate 3, manufactured by Thoratec Corp., a subsidiary of Abbott Laboratories, have been linked to at least 14 deaths and over 4,500 reports of potential harm. These mechanical heart pumps are crucial for patients with end-stage heart failure who are awaiting a transplant or …

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Medical Devices Recalled by Health Canada, OmniLab Advanced Warning issued for Potentially Fatal Flaw

Health Canada has issued recalls for several medical devices, raising concerns about potential risks to patients. One of the devices flagged is the OmniLab Advanced, commonly used by individuals with sleep apnea, a condition that disrupts breathing during sleep. The device has been reported to have internal errors or malfunctions that could lead to therapy interruptions, posing serious risks to patients, including possible respiratory failure and even death in vulnerable individuals. In addition to the …

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Explosion-Protected Devices Unveiled by Axis Communications in Industry First

Boston, MA – Axis Communications has recently revealed the world’s first explosion-protected devices, marking a significant advancement in security technology. These innovative devices are designed to enhance safety and security in high-risk environments where explosions are a potential threat. The new explosion-protected devices from Axis Communications are set to revolutionize the way security systems operate in hazardous areas such as oil refineries, chemical plants, and other industrial settings. By providing robust protection against explosions, these …

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