MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION COMPELLA BARIATRIC BED

Model Number	P7800A
Medical Device Problem Code	Material Split, Cut or Torn (4008)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/24/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The baxter technician found the power cord needed to be replaced.Per the hillrom service manual it is necessary for the compella bariatric bed to have an effective maintenance program.We recommend that you do annual preventive maintenance.Pay particular attention to safety features, which include but are not limited to, the power cords for the bed and asu are with the unit, and they are in good condition, the plug is a one piece molded plug assembly, the assembly shows no signs of cracking, the plug molding around the blade is not discoloured and the blade is tight in the molding.The power cord hooks shows no sign of cracking and are intact with no damage.Replace or repair parts as necessary.A search of the baxter maintenance records did not show baxter performed any preventative maintenance on this bed.It is unknown if they facilty perfoms preventative maintenace on their beds.The technincan replaced the power cord to resolve the reported event.Based on ths inforamiton, no further actions is required.
Event or Problem Description
During servicing by baxter, technical service identified that compella rent us scale pd ppm had power cord copper exposed.There was no patient/user injury, medical intervention, symptom, or adverse event reported.

• Brand Name: COMPELLA BARIATRIC BED
• Common Device Name: BARIATRIC BED
• 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: 25238282
• Report Number: 1824206-2026-01150
• Device Sequence Number: 21469702
• Product Code: OSI
• UDI-Device Identifier: 00887761000902
• UDI-Public: (01)00887761000902(11)190213
• Combination Product (Y/N): N
• Initial Reporter State: CA
• 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): 05/21/2026

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
• Device Model Number: P7800A
• Device Catalogue Number: P7800ARENT01
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/24/2026
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/24/2026
• Initial Report FDA Received Date: 05/21/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/13/2019
• 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