MAUDE Adverse Event Report: STRETCHER; STRETCHER, WHEELED

Device Problem Output Problem (3005)

Patient Problem Insufficient Information (4580)

Event Date 07/01/2021

Event Type  malfunction  

Event Description

Healthcare provider made the comment that when moving patients on stretcher surfaces the bedsheets would move around and would require them to have to manually pull them back up to the top.No indication of injury or issues other than being a repeated inconvenience.Fda safety report id# (b)(4).

• Brand Name: STRETCHER
• Type of Device: STRETCHER, WHEELED
• MDR Report Key: 12135192
• MDR Text Key: 260605578
• Report Number: MW5102344
• Device Sequence Number: 1
• Product Code: FPO
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 07/01/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/06/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: No Information
• Was Device Available for Evaluation?: No
• Was Device Evaluated by Manufacturer?: No Information
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Age: 33 YR