Incident reporting deadlines and obligations
Some incidents start a clock; these pages say which ones, who must be told, and by when.
Start here.
- 42 CFR 483.12(B)(5) AND (C); SECTION 1150B OF THE SOCIAL SECURITY ACT; F607, F609, F610
Nursing home abuse and neglect reporting requirements
Federal rules give nursing homes two clocks. Report alleged abuse, or any allegation that causes serious bodily injury, immediately and within 2 hours. Report other alleged violations within 24 hours. Send investigation results within 5 working days of the incident.
CMSRead the guide - JOINT COMMISSION SENTINEL EVENT POLICY (SE CHAPTER, COMPREHENSIVE ACCREDITATION MANUAL FOR HOSPITALS, JULY 2026 UPDATE)
Joint Commission sentinel event policy: what to do and by when
A sentinel event is a patient safety event that reaches a patient and results in death, severe harm or permanent harm. Reporting it to Joint Commission is encouraged, not required. Each one needs a full analysis and action plan within 45 business days of the event or of becoming aware of it.
The Joint CommissionRead the guide - 42 CFR 416.300 THROUGH 416.320; SECTION 1833(I)(7) OF THE SOCIAL SECURITY ACT
ASC Quality Reporting Program (ASCQR): measures, deadlines and penalty
The ASC Quality Reporting Program is a CMS pay-for-reporting program. An ASC that misses its requirements gets a 2.0 percentage point cut to its Medicare annual payment update. Data for 2026 are due January 1 to May 17, 2027 and affect 2028 payment. OAS CAHPS survey data are due quarterly.
CMSRead the guide - 21 CFR PART 803, SUBPART C (803.30, 803.32, 803.33), WITH 803.17 AND 803.18
FDA medical device reporting for user facilities
Under 21 CFR Part 803, a device user facility must report a device-related death to FDA and the manufacturer. The deadline is 10 work days from becoming aware. It reports a serious injury to the manufacturer, or to FDA if the manufacturer is unknown, in the same time. A facility that filed any reports also sends FDA an annual report on Form FDA 3419 by January 1.
FDA (Center for Devices and Radiological Health)Read the guide - STATE STATUTES AND REGULATIONS (VARY BY STATE); FEDERAL FLOOR FOR NURSING HOMES AT 42 CFR 483.12
State adverse event and incident reporting: a verified overview
Most states run their own adverse event reporting system. Rules differ on who reports, what counts and how fast. This page covers four verified systems, not every state: Pennsylvania, New York, Minnesota and Florida. Confirm yours with your licensing agency.
State health departments and designated state agenciesRead the guide
Map every rule to the record.
IncidentKit connects each requirement to the incident, the investigation and the corrective action that satisfy it.