McKesson—Anesthesia Care Systems: Case Data May Not Match Patient Data

ECRI Institute's complete weekly summary of medical device hazard and recall information is available in ECRI Institute's Health Devices Alerts(HDA). For more information about HDA, contact us at clientservices@ecri.org.

FDA's Center for Devices and Radiological Health (CDRH) states that the systems below may not correctly match patient data to later patient case data in the Anesthesia Care Record (ACR) and may include data from a different patient when it is recalled. FDA's CDRH also states that the manufacturer initiated a...