MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION CENTRELLA BED; BED, AC-POWERED ADJUSTABLE HOSPITAL

Model Number	P7900A
Medical Device Problem Code	Defective Alarm (1014)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/20/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The baxter technician found the nurse call cable needed to be replaced.Per the baxter service manual, it is necessary for the centrella bed to have an effective maintenance program.We recommend that you do annual preventative maintenance pm.Make sure the bed exit system operates correctly.Replace parts if necessary.A search of the baxter maintenance records showed baxter performed preventive maintenance on this bed on jul 15, 2025.It is unknown if the facility performed any other preventive maintenance on this bed.The technician replaced the nurse call cable to resolve the reported event.Based on this information, no further action is required.
Event or Problem Description
On 20-jan-2026, a customer contacted technical service to report that centrella frame (product code p7900a000009, serial number (b)(6)), had bed exit alarm not alarming at the nurse's station.The process step during which this occurred was unknown.There was no patient/user injury, medical intervention, symptom, or adverse event reported.

• Brand Name: CENTRELLA 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: 24367232
• Report Number: 1824206-2026-00376
• Device Sequence Number: 20137381
• Product Code: FNL
• UDI-Device Identifier: 00887761999961
• UDI-Public: (01)00887761999961(11)171006
• Combination Product (Y/N): N
• Initial Reporter State: NC
• 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): 02/17/2026

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: P7900A
• Device Catalogue Number: P7900A000009
• Device Lot Number: N/A
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/21/2026
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/20/2026
• Initial Report FDA Received Date: 02/17/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 10/05/2017
• 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