EHR recall: Use of this affected product may cause serious adverse health consequences, including death

Here is another example of a grossly defective health IT product, this from last year but only posted by FDA publicly on 3/14/2014 at http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm389356.htm: "There was an occurrence where the patient case data did not match the patient data when the case was recalled in the Anesthesia Care Record (ACR) in that it included data from another case. Use of this affected product may cause serious adverse health consequences, including death."One wonders why problems like this are found in the field when real patients are involved, not in the testing lab...could it have to do with lack of regulatory oversight?Other examples of recalled bad health IT that I know of, including FDA-initiated recalls, are here:  http://hcrenewal.blogspot.com/2012/07/health-it-fda-recall-philips-xcelera.html, http://hcrenewal.blogspot.com/2011/12/fda-recalls-health-it-software-because.html , http://hcrenewal.blogspot.com/2013/08/a-good-way-to-cynernetically-harm-or.html. Also note the FDA advisory:  Health care professionals and consumers may report adverse reactions or quality problems they experienced using these products to MedWatch: The FDA Safety Information and Adverse Event Reporting Program either online, by regular mail or by FAX:http://www.fda.gov/MedicalDevices/Safety/ListofRecalls/ucm389328.htm McKesson Technologies, McKesson Anesthesia Care – Patient Case Data May Not Match Patient DataR...
Source: Health Care Renewal - Category: Health Medicine and Bioethics Commentators Tags: FDA recall healthcare IT defects healthcare IT risk McKesson McKesson Anesthesia Care Source Type: blogs