Inspection Reports for Revela at O’Fallon

The inspection was conducted as a complaint investigation for the Revela at O'Fallon facility.

The facility was found to be in compliance with Part 295 Assisted Living and Shared Housing Establishment Administrative Code and 210 ILCS 9/1 Assisted Living and Shared Housing Act.

Complaint Investigation 25411494 IL198708 concluded with the facility in compliance.

Annual Licensure Survey to assess compliance with Part 295 Assisted Living and Shared Housing Establishment Administrative Code and 210 ILCS 9/1 Assisted Living and Shared Housing Act.

The establishment was found to be in compliance with the applicable assisted living and shared housing regulations during the annual licensure survey.

The inspection was conducted in response to a complaint (IL187022) regarding medication administration errors at the facility.

The facility failed to ensure residents received the correct medication, resulting in resident R1 not receiving their prescribed medication and receiving an incorrect medication on 02/11/25. The error was identified immediately, no adverse reaction occurred, and corrective actions including retraining and removal of the employee from medication administration were taken.

Complaint IL187022 triggered the investigation. The complaint was substantiated by findings of medication errors involving resident R1.

The inspection was conducted in response to a complaint (Complaint #2541529/IL187022) regarding medication administration errors at Revela at O'Fallon.

The establishment failed to meet the requirements of Section 295.5000 related to medication reminders, supervision of self-medication, medication administration, and storage. A medication error was reported involving a staff member (E8), who was disciplined and the medication policy was reviewed with staff. Medication administration observations were conducted with no interruptions or chart omissions noted during the medication pass.

Complaint #2541529/IL187022 was substantiated with a Type 2 citation for medication administration errors. The medication error was immediately reported, and corrective actions including staff discipline and policy review were implemented.

The inspection was conducted as an Annual Licensure Survey to assess compliance with regulatory requirements.

The facility was found to be non-compliant with Section 295.2040 Disaster Preparedness due to failure to orient residents to emergency and evacuation plans within ten days of admission, with no documentation of such orientation available.

The inspection was conducted as an Annual Licensure Survey to assess compliance with regulatory requirements.

The facility was found to have a Type 3 violation related to disaster preparedness, specifically failing to ensure residents received orientation to emergency and evacuation plans within ten days of admission.