Standardized Documentation for Adverse Events and Near Misses
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□ Wrong Site/Side/Patient □ Equipment Malfunction □ Medication Error □ Sterility Breach □ Unexpected Bleeding □ CPB-related Incident □ Airway Management Issue □ Other: ________________
□ Near Miss □ No Harm □ Mild Harm □ Moderate Harm □ Severe Harm □ Death
Detailed account of the incident:
□ Patient/Family Notified □ Risk Management Notified □ Root Cause Analysis Required □ M&M Conference Review
Recommendations to prevent recurrence:
Form ID: CS-IR-[YYYY]-[###]
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