MAUDE Adverse Event Report: HILL-ROM, INC. STRETCHER; STRETCHER, WHEELED

Device Problem Component Missing (2306)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

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 hill-rom stretcher, serial number (b)(6), had hardware missing on bar handles and hand siderails were missing causing them to fall down.(b)(4).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
• Manufacturer (Section D): HILL-ROM, INC.
• MDR Report Key: 17526042
• MDR Text Key: 321343666
• Report Number: MW5132982
• 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: 11/29/2017

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
• Patient Sequence Number: 1