MAUDE Adverse Event Report: STRETCHER; STRETCHER, WHEELED

Device Problems Mechanical Problem (1384); Component Missing (2306)

Patient Problem Insufficient Information (4580)

Event Type  malfunction  

Event Description

Stryker medical was notified of a potentially reportable complaint involving a product for which stryker is not the original equipment manufacturer of the reported device.The customer alleged a manufacturer stryker stretcher, serial number (b)(6) that had brakes that would not remain engaged, and one brake pedal was missing.Please find additional contact information below.This report reflects information received by fda in the form of a notification per 803.22 (b)(2).

• Brand Name: STRETCHER
• Type of Device: STRETCHER, WHEELED
• MDR Report Key: 17317485
• MDR Text Key: 319064422
• Report Number: MW5119372
• Device Sequence Number: 1
• Product Code: FPO
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 06/29/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/12/2023
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Patient Sequence Number: 1