Audiovisual Recalls and safety alerts affecting automated external defibrillators. Citation Text: Shah JS, Maisel WH. Recalls and safety alerts affecting automated external defibrillators. JAMA. 2006;296(6):655-60. Copy Citation Format: Google ScholarPubMedBibTeXEndNote X3 XMLEndNote 7 XMLEndnote taggedPubMedIdRIS Download Citation Save Save to your library Print Share Facebook Twitter Linkedin Copy URL August 23, 2006 Shah JS, Maisel WH. JAMA. 2006;296(6):655-60. View more articles from the same authors. The authors analyzed recall and safety alerts for automated external defibrillators and found that advisories occur frequently, and actual malfunctions occur occasionally. PubMed citation Available at Free full text Save Save to your library Print Share Facebook Twitter Linkedin Copy URL Cite Citation Citation Text: Shah JS, Maisel WH. Recalls and safety alerts affecting automated external defibrillators. JAMA. 2006;296(6):655-60. 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March 13, 2019 View More See More About The Topic Safety Scientists Engineers Epidemiology of Errors and Adverse Events Medical Device Design
Mobile physician reporting of clinically significant events—a novel way to improve handoff communication and supervision of resident on call activities. December 3, 2014
Seroprevalence of SARS-CoV-2 among frontline health care personnel in a multistate hospital network--13 academic medical centers, April-June 2020. September 23, 2020
Effect of restriction of the number of concurrently open records in an electronic health record on wrong-patient order errors: a randomized clinical trial. May 29, 2019
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Duke Surgery Patient Safety: an open-source application for anonymous reporting of adverse and near-miss surgical events. May 16, 2007
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Quality and Safety Considerations in Intensity Modulated Radiation Therapy: An ASTRO Safety White Paper Update. May 17, 2023
More than algorithms: an analysis of safety events involving ML-enabled medical devices reported to the FDA. May 3, 2023
Effects of racial bias in pulse oximetry on children and how to address algorithmic bias in clinical medicine. April 5, 2023
Use of recalled devices in new device authorizations under the US Food and Drug Administration's 510(k) pathway and risk of subsequent recalls. January 25, 2023
Developing strategic recommendations for implementing smart pumps in advanced healthcare systems to improve intravenous medication safety. November 16, 2022
Pulse oximeters and their inaccuracies will get FDA scrutiny today. What took so long? November 9, 2022
Can the standard configuration of a cardiac monitor lead to medical errors under a stress induction? July 27, 2022
FDA Safety Communication: flexible bronchoscopes and updated recommendations for reprocessing. February 24, 2022 - February 24, 2022
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