Final HAN 382 Medical Device Reprocessing Reminder 09112015

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Posted: Friday, September 11, 2015 2:52 PM

 

The Centers for Disease Control and Prevention (CDC) and U.S. Food and Drug Administration (FDA)
are alerting healthcare providers and facilities about the public health need to properly maintain, clean,
and disinfect or sterilize reusable medical devices. Recent infection control lapses due to non-compliance
with recommended reprocessing procedures highlight a critical gap in patient safety. Healthcare facilities
(e.g., hospitals, ambulatory surgical centers, clinics, and doctors' offices) that utilize reusable medical
devices are urged 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.

The Centers for Disease Control and Prevention (CDC) and U.S. Food and Drug Administration (FDA) are alerting healthcare providers and facilities about the public health need to properly maintain, clean, and disinfect or sterilize reusable medical devices. Recent infection control lapses due to non-compliance with recommended reprocessing procedures highlight a critical gap in patient safety. Healthcare facilities (e.g., hospitals, ambulatory surgical centers, clinics, and doctors' offices) that utilize reusable medical devices are urged 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.

 

For more information and to see the full text of CDC Advisory Final HAN 382 Medical Device Reprocessing Reminder 09112015 click on this text.