MAUDE Adverse Event Report: HILL-ROM STRETCHER, WHEELED

Model Number P8000

Device Problem Break (1069)

Patient Problem Insufficient Information (4580)

Event Type  malfunction  

Event Description

A hill rom p8000 stretcher, serial number (b)(6) had a broken side rail.(b)(4).This report reflects information received by fda in the form of a notification per 803.22 (b)(2).

• Brand Name: STRETCHER, WHEELED
• Type of Device: STRETCHER, WHEELED
• Manufacturer (Section D): HILL-ROM
• MDR Report Key: 17527802
• MDR Text Key: 321326476
• Report Number: MW5134733
• Device Sequence Number: 1
• Product Code: FPO
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 02/19/2015

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/12/2023
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: No
• Device Model Number: P8000
• Patient Sequence Number: 1