MAUDE Adverse Event Report: HAUSTED STRETCHER, WHEELED

Model Number 462CPAST

Device Problem Break (1069)

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 husted 462cpast, serial number not available, the pl siderail is broken.(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): HAUSTED
• MDR Report Key: 17525962
• MDR Text Key: 321343642
• Report Number: MW5132902
• 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: 06/05/2014

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: 462CPAST
• Patient Sequence Number: 1