MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION HILL-ROM RESIDENT LONG TERM CARE BED; BED, AC-POWERED ADJUSTABLE HOSPITAL

Model Number	P870C
Medical Device Problem Code	Positioning Failure (1158)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/26/2026
Type of Reportable Event	Malfunction
Event or Problem Description
On 26-jan-2026, a other health care professional contacted technical service to report that resident bed (product code p870cb4851, serial number (b)(6)), the head of the bed moves on its own.There was no patient/user injury, medical intervention, symptom, or adverse event reported.
Additional Manufacturer Narrative
The baxter technical support representative performed troubleshooting over the phone with the account, asking the account to replace the head actuator connector with knee.Per the baxter service manual, it is necessary for the resident ltc bed to have an effective maintenance program.We recommend that you do annual preventive maintenance.Test each operating function individually to make sure that when pressed, the corresponding function operates correctly and when released, travel stops.A search of the baxter maintenance records did not show baxter performed any preventative maintenance on this bed.It is unknown if the facility performs preventative maintenance on their beds.The account will replace the bed no further action needed.

• Brand Name: HILL-ROM RESIDENT LONG TERM CARE BED
• Common Device Name: BED, AC-POWERED ADJUSTABLE HOSPITAL
• Manufacturer (Section D): BAXTER HEALTHCARE CORPORATION; deerfield IL
• Manufacturer (Section G): HILL-ROM BATESVILLE; 1069 state route 46 east; batesville IN 47006
• Manufacturer Contact: 25212 w. illinois route 120; round lake, IL 60073 ; 2242705355
• MDR Report Key: 24423359
• Report Number: 1824206-2026-00417
• Device Sequence Number: 18792870
• Product Code: FNL
• UDI-Device Identifier: 00887761000926
• UDI-Public: (01)00887761000926(11)030720
• Combination Product (Y/N): N
• Initial Reporter State: WI
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 02/23/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Other
• Device Model Number: P870C
• Device Catalogue Number: P870CB4851
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/26/2026
• Initial Report FDA Received Date: 02/23/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 07/20/2003
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown