MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION HILL-ROM 100 LOW BED; BED, AC-POWERED ADJUSTABLE HOSPITAL

Model Number	P3930A
Medical Device Problem Code	Unintended Movement (3026)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/20/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The baxter technician found the casters needed to be replaced.Per the baxter service manual: do a periodic inspection to make sure all bed functions operate correctly, especially the safety features.Safety features include, but are not limited, to these: ¿ connectors where the bed sections bolt together; tighten as necessary.¿ siderail latching mechanisms.¿ caster braking systems.A search of the baxter maintenance records showed baxter performed preventative maintenance on this bed in aug 29, 2023.It is unknown if the facility performed any other preventative maintenance on this bed.The technician replaced the end foot casters to resolve the reported event.Based on this information, no further action is required.
Event or Problem Description
On 20-feb-2026, a company representative - service personnel contacted technical service to report that gpac frame-assembled (product code p3930a000026, serial number (b)(6)), had brakes would not hold while in brake.This occurred after patient use.There was no patient/user injury, medical intervention, symptom, or adverse event reported.

• Brand Name: HILL-ROM 100 LOW 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: 24644045
• Report Number: 1824206-2026-00649
• Device Sequence Number: 15926599
• Product Code: FNL
• UDI-Device Identifier: 00887761000919
• UDI-Public: (01)00887761000919(11)101021
• Combination Product (Y/N): N
• Initial Reporter State: HI
• 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: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 03/19/2026

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: P3930A
• Device Catalogue Number: P3930A000026
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 02/20/2026
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/20/2026
• Initial Report FDA Received Date: 03/19/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 10/21/2010
• 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