MAUDE Adverse Event Report: HILL-ROM, INC. PROGRESSA BED SYSTEM; BED, AC-POWERED ADJUSTABLE HOSPITAL

Model Number P7500A

Device Problem Failure to Power Up (1476)

Patient Problem Insufficient Information (4580)

Event Date 05/19/2023

Event Type  malfunction  

Event Description

Monitor and hill-rom bed will not turn on.Manufacturer response for bed, ac-powered adjustable hospital, progressa bed system (per site reporter).Work order was placed and waiting for response.

• Brand Name: PROGRESSA BED SYSTEM
• Type of Device: BED, AC-POWERED ADJUSTABLE HOSPITAL
• Manufacturer (Section D): HILL-ROM, INC.; 1069 state route 46 east; batesville IN 47006
• MDR Report Key: 17078117
• MDR Text Key: 316675667
• Report Number: 17078117
• Device Sequence Number: 1
• Product Code: FNL
• UDI-Device Identifier: 00887761000100
• UDI-Public: (01)00887761000100
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: User Facility
• Reporter Occupation: Nurse
• Type of Report: Initial
• Report Date: 06/01/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 06/07/2023
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: P7500A
• Device Catalogue Number: P7500A000744
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Date Report Sent to FDA: 06/01/2023
• Device Age: 5 YR
• Event Location: Hospital
• Date Report to Manufacturer: 06/07/2023
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1