Magnolia Ridge ALF was inspected 8 times between April 21, 2021 and May 18, 2026 by the Virginia Department of Social Services. 6 of those visits ended with violations cited and 2 with none. Across that history VDSS cited 35 violations under 26 distinct standards. 1 inspection was prompted by a complaint.
A violation is a licensing standard - a rule in the Virginia Administrative Code - that the inspector found the facility was not meeting. Each is shown with the evidence the inspector recorded and, where VDSS publishes it, the facility's own plan of correction.
VDSS publishes inspections on a rolling window. 7 of these 8 are still on the state's site; the other 1 has since dropped off it and is reproduced from Assisted Living Magazine's archive of the original VDSS reports.
Provider Information
Inspection History
8Select an inspection to read the areas reviewed, the inspector's comments and any violations cited.
May 18, 2026Inspection
- The record for resident 4 has documentation that the resident receives services from a mental health provider. In an interview with staff persons 1 and 4, it was reported that this was accurate. The ISP dated 07/31/2025 in the record for resident 4 does not include the identified need for mental health services.
- The record for staff persons 1 and 2, who were transfer employees from another facility in 2025, did not contain documentation that these employees had received orientation and training specific to this facility. In an interview with staff persons 1 and 4 it was reported that this was correct.
- The record for resident 1 has documentation that the last risk assessment for tuberculosis for this resident was completed on 02/28/2025.
- The record for resident 4 has documentation that the last risk assessment for tuberculosis for this resident was completed on 03/24/2025.
- The record for resident 3, admitted to the facility on 12/12/2025, did not contain documentation that the facility completed a sex offender screening prior to the residents admission to the facility.
- The facility MMP has documentation that “verification of accurate transcription of medication orders to the MAR within 24 hours of receipt of a new order or change in an order shall be verified by the arriving med aide and the administrator”.
- The record for resident 4 has a physician order dated 01/21/2026 for Urea 40% cream apply a sufficient amount daily to rough skin areas on both heels. The medication observed in the cart for resident 4 was Urea 40% cream but the May 2026 MAR for resident 4 has documentation of Urea 20% cream.
- The record for resident 1 has documentation of a physician order for Invega Sustenna 234mg injection to be administered every 4 weeks. The April and May 2026 MARs for resident 1 do not have documentation of this medication being administered. In an interview with staff person 1, it was report that this injection is administered monthly at resident 1’s physicians office but the record for resident 1 does not have documentation of the administration of the medication.
April 29, 2025Inspection
- The record for resident 1 has documentation of a mental health progress report dated 03/07/2025 that the resident needs continued mental health services. The ISP dated 11/03/2024 in the record for resident 1 does not address the identified need for mental health services.
- The record for resident 3 has documentation of a mental health progress report dated 04/23/2025 that the resident needs continued mental health services. The uniform assessment instrument (UAI) dated 02/10/2025 has documentation that resident 3 uses bed rails for mobility. The ISP dated 02/10/2025 in the record for resident 3 does not address the identified need for mental health services or bed rails for mobility.
- The facility fire drill log made available for review on 04/29/2025, the day of on-site inspection, did not include documentation of a drill being conducted for any shift for March 2025.
- A opened Novolog Flex Pen and a opened Insulin Glargine-yfgn Pen were observed sitting out on the top of the medication cart at 9:21am on the day of on-site inspection. The pens did not contain a pharmacy issued label or the name of the resident that the medication is for.
- The 3 light fixtures in the hallway between rooms 9 through 12 were inoperable on the day of on-site inspection.
- The most recent health care over sight provided for review on 04/29/2025, the day of on-site inspection, was dated 12/14/2024, which is past the three-month requirement for residents residing in the facility who are assessed for assisted living level of care.
- The record for resident 1 has documentation of a physician order dated 04/23/2025 for Potassium Chl 20meq daily and Furosemide 20mg daily. The April 2025 medication administration record (MAR) for resident 1 has documentation that the Furomeside 20mg was not started until 04/28/2025 and the Potassium 20meq was not documented on the MAR. The Potassium was noted to not be available in the facility for resident 1 on the day of on-site inspection. An interview with staff person 4 on the day of on-site inspection expressed that the Furosemide 20mg was not started until 04/28/2025 because that is when it was received from the pharmacy and the Potassium medication has not been administered because it has not been received from the pharmacy.
- The record for resident 1 has a physician order dated 01/17/2025 for Ferrous Sulfate 325mg daily for 90 days then stop. The April 2025 MAR for resident 1 has staff initials for the administration of this medication from 04/18/2025 through 04/29/2025 even though the 90-day time frame ended on 04/17/2025.
- The record for resident 2 has a physician order dated 02/27/2025 for Fluticas 250/ Salmeterol 50 Inhl Disk, inhale 1 inhalation by mouth twice a day. Rinse mouth after each use to prevent oral thrush. The April 2025 MAR for resident 2 does not have documentation of the mouth rinse after each use of this medication.
- The record for resident 3 has a physician order dated 12/18/2024 for Ferrous Sulfate 325mg daily for 90. The April 2025 MAR for resident 3 has staff initials for the administration of this medication from 04/01/2025 through 04/29/2025 even though the 90-day time frame ended on 03/18/2025.
- The facility MMP has documentation on page 5 that “Controlled substances must be kept under double locks; controlled substances must be counted at the end of each shift and documented by two med-aides”.
- The February and March 2025 12-Hour Controlled Drugs-Count Record has multiple days/shifts that do not have documentation of staff signatures for the counting of controlled substances.
- The record for resident 4 has a physician order for blood sugars 4 times a day before meals and at bedtime before giving insulin. The Blood glucose monitoring form for April 2025 does not have documentation of resident 4’s blood sugar results at pre-dinner on 04/01/2025.
February 4, 2025Complaint survey
May 3, 2024Inspection
- The April 2024 MAR for resident 3 has documentation of the PRN medication Lorazepam 0.25ml every 4 hours as needed for anxiety being administered on 04/07/2024 and 04/12/2024 and the PRN medication Morphine Sulf 0.25ml every 4 hours as needed for pain being administered on 04/06/2024 and 04/07/2024. The MAR does not have documentation of the effectiveness of these medications for the doses that were administered.
- The alarms on the doors leading to the outside next to rooms 12 and 27 were not operable on the day of inspection. The facility houses a mixed population of residents such as resident 2 who has a diagnosis of Dementia, is assessed as non-ambulatory on a history and physical dated 03/21/2023 and is marked as disoriented to some spheres some of the time with time and place being the spheres affected on a uniform assessment instrument (UAI) dated 02/08/2024.
- The records for residents 2, 3 and 5 have documentation that the last review of medications for these residents was completed on 10/05/2023. All 3 of these residents are assessed as assisted living level of care on their uniform assessment instruments (UAI).
- The record for resident 4, admitted on 03/22/2024, has documentation on the physical examination dated 03/20/2024 that resident 4 has the prohibited conditions, psychotropic medications without appropriate diagnosis and treatment plans and requires continuous licensed nursing care., making it unclear if this resident is appropriate for placement in an assisted living facility.
- The storage closet next to room 18 was observed to be unlocked on the day of inspection and contained 2 boxes of Lidocaine 5% patches sitting out on a shelf in the closet.
April 19, 2023Inspection
- At 9:22am on the day of inspection a electric space heater was observed on and in use in room 17.
- On the day of inspection a bottle of Advil PM and a bottle of Excedrin Migraine were observed sitting out on the top of a dresser in the room for resident 6. A review of the UAI dated 10/10/2022 in the record for resident 6 has documentation that the facility administers medications to resident 6. There was no documentation of a physician order for these medications in resident 6’s record.
- The record for resident 4 has documentation that the last fall risk rating completed for this resident was dated 01/07/2022. The uniform assessment instrument (UAI) dated 01/05/2023 in the record for resident 4 has documentation that the resident is assessed as assisted living level of care.
- The record for resident 6 has documentation that the resident receives mental health services. The ISP dated 11/06/2022 does not address this identified need.
- The record for staff person 1, hired on 10/30/2006, has documentation that the last screening for tuberculosis was completed on 10/07/2021.
- The light fixture above the medication room was noted to be hanging loose from the ceiling on one side.
- The light fixture above the sink in room 17 was missing and the light was inoperable after flipping on the corresponding light switch.
- During the day of inspection both LI’s were unable to locate the pendant device for the facility signaling system for room 9, 12, 14, 17, 21, and 22. A signaling device pendant located in room 31 was pushed by the LI but it alerted to the signaling box that it was room 12. Interview with residents expressed that they do not have signaling devices in their rooms. Interview with staff 3 expressed that residents frequently remove the signaling pendant devices from their rooms and then lose them.
August 4, 2022Inspection
May 10, 2022Inspection
- On the day of inspection 3 Lantus Solostar pens and 1 Novolog Flexpen was observed in the medication refrigerator for resident 3, who had passed away on 02/26/2022. The facility medication management plan has documentation that it is the facility’s best practice to return all expired and discontinued medications to the pharmacy.
- An open bottle of Lantus insulin was observed in the medication refrigerator for resident 1 on the day of inspection. The bottle did not contain a date that the insulin was opened to ensure that it is discarded within 28 days of opening per manufacturer’s instructions. The facility medication management plan has documentation to check expiration dates before administering monthly and before each med pass.
- The most recent health care oversight available for review was dated 01/09/2022. The facility houses residents who are assessed at an assisted living level of care which require a healthcare oversight every 3 months.
- The record for resident 2 has documentation of a physician order dated 05/23/2019 for a No Added Sweets diet.
- The record for resident 3 has documentation of a physician order dated 10/20/2021 for a No Concentrated Sweets diet.
- The mid-day meal was observed at 12:11pm on the day of inspection in the presence of staff person 5. It was noted that a hamburger with lettuce, tomato and onion, tator tots, and white cake with icing was served to all resident in the dining room including residents 1 and 2. An interview was conducted with staff person 4 on the day of inspection in which it was expressed that the cake that was served during the mid-day meal was a regular cake with icing. The LI asked staff person 4 if a reduced or sugar free desert option was available for residents who have diets requiring No Added Sweets or No Concentrated Sweets. Staff person 4 expressed that there are sugar free deserts available but that they had not been served to residents 2 or 3 at the mid-day meal on the day of inspection.
- A paper soufflé cup with 1 whole and 1 half white pill was observed to be sitting out on the shelf in the medication room.
- 3 white pills were observed to be lying loose in the bottom of the third drawer of the medication cart.
- An unlabeled glucometer was observed lying on top of the medication cart on the day of inspection.
- An unlabeled glucometer was observed in the right top drawer on the medication cart.
- A bag labeled with resident 8’s name was noted in the medication cart. The glucometer inside of the bag was unlabeled.
- A multi-stick penlet device was observed lying on top of the medication cart on the day of inspection. An interview conducted with staff person 2 on the day of inspection expressed that the facility currently did not have any single use safety lancets for assisted blood glucose monitoring and that the multi-stick penlet lying on top of the medication cart had been used to check blood glucoses for both residents 1 and 2 that morning.
- At 9:20am on the day of inspections it was observed that the sliding glass window in the door to the facility medication room was unlocked. The LI was able to reach their hand through the window and open the door to the medication room. The room was unoccupied and contained a shelf with numerous medications for multiple residents sitting on the shelf. The facility medication cart, which contained various medications for multiple residents was also stored in this room and was observed to be unlocked.
- The ceiling lights in the hallway outside of rooms 10, 20, 27, the visitor/employee bathroom and the Administrators office were noted to be inoperable on the day of inspection.
- A bottle of Chlorhexidine Gluconate Mouth Wash was observed sitting out on a dresser in the room for resident 3 on the day of inspection. An interview with resident 3 expressed that he uses this mouth wash himself twice a day.
- The uniform assessment instrument (UAI) dated 01/09/2022 in the record for resident 3 has documentation that the resident requires medication administration from a layperson. The physician order in resident 3’s record for the Chlorhexidine Gluconate Mouth Wash dated 04/18/2022 does not have instructions that the resident can self-administer this prescribed medication.
April 21, 2021Inspection
- The facility medication management plan did not include procedures for the facility standard dosing times, ensure that residents do not receive medications or dietary supplements to which they have known allergies, or procedures for identification of the medication aide or the person licensed to administer drugs responsible for routinely communicating issues or observations related to medication administration to the prescribing physician or other prescriber;