Adverse Events from Robotic Surgery – Under-reported?

January 6, 2014    |   By: Calevir

The FDA is evaluating its system for reporting of device-related events based on concerns of under-reporting, specifically of robotic surgery related adverse events.   Studies reveal most of these events are not reported until after some type of legal action occurs.   The ideal is to identify these events when they occur, in time to take preventive action and to report those events so an analysis can be performed and prevention efforts shared across the industry.   Read more


PSO Case Law: Ungurian v. Beyzman, et al., 2020 PA Super 105:

A recent Pennsylvania case shows how courts narrowly interpret the PSQIA, ignoring the D & A pathway and the clear language of the Final Rule. (Ungurian v. Beyzman, et al., 2020 PA Super 105). The cour

Joint Commission New Sentinel Event Alert 61: Managing the Risks of Direct Oral Anticoagulants:

The Center for Patient Safety wants to share this important harm-prevention advice from The Joint Commission and its Sentinel Event Alert: Managing the Risks of Direct Oral Anticoagulants. The Joint Commis

CPS Safety Watch/Alert – Culture Can Improve the Control of Multi-Drug Resistant Organisms:

Issue: A number of events reported co CPS’ Patient Safety Organization (PSO) demonstrate poor handoff communication about the patients’ infectious disease status Examples include: Patient with

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