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As a result, these sophisticated devices are frequently linked to the harm done to patients, which is in stark contrast to the situation described above. According to the Food and Drug Administration of the United States of America, between 2005 and 2009, infusion pumps were recalled due to safety concerns due to the agency's findings. The FDA discovered that the complexity of the pumps was responsible for 56,000 adverse drug events, some of which were harmful or fatal, over the course of that time period. These recurring incidents, ... more