Review current reprocessing practices

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Reference no: EM133623837

Question

Why did the CDC and the FDA issue a Health Advisory in 2015 urging all healthcare facilities to immediately review current reprocessing practices at their facility to ensure they (1) are complying with all steps as directed by the device manufacturers, and (2) have in place appropriate policies and procedures that are consistent with current standards and guidelines? Group of answer choices Recent infection control lapses due to noncompliance with recommended medical device reprocessing procedures highlighted a critical gap in patient safety. It was part of a 10-year plan to boost patient safety practices. Both agencies just developed new guidelines or regulations on instrument processing in healthcare facilities. A new director of the CDC and a new Commissioner of the FDA were just appointed.

Reference no: EM133623837

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