MAUDE Adverse Event Report: UNKNOWN STERIS STRETCHER; STRETCHER, WHEELED

Device Problems Fluid/Blood Leak (1250); Unintended System Motion (1430)

Patient Problem Insufficient Information (4580)

Event Type  malfunction  

Event Description

On february 22, 2012, stryker medical was notified of a potentially reportable complaint involving a product for which stryker is not the manufacturer.The customer reported a steris stretcher, product serial number (b)(6), had a drifting fowler cylinder and a leaking jack.Please find additional contact information below.N/a.This report reflects information received by fda in the form of a notification per 803.22 (b)(2).

• Brand Name: STERIS STRETCHER
• Type of Device: STRETCHER, WHEELED
• Manufacturer (Section D): UNKNOWN
• MDR Report Key: 17533408
• MDR Text Key: 321189482
• Report Number: MW5140312
• 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: 03/21/2012

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