MAUDE Adverse Event Report: FERNO STRETCHER, WHEELED

Device Problems Break (1069); Naturally Worn (2988)

Patient Problem Insufficient Information (4580)

Event Type  malfunction  

Event Description

On (b)(6) 2011, stryker medical was notified of a potentially reportable complaint involving a product for which stryker is not the manufacturer.It was reported through service report that a ferno ambulance cot 93es, serial number (b)(6), had worn and broken springs, the o2 holder plate was broken, and the pusher, release cable, and bearings were worn.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, WHEELED
• Type of Device: STRETCHER, WHEELED
• Manufacturer (Section D): FERNO
• MDR Report Key: 17533715
• MDR Text Key: 321273419
• Report Number: MW5140619
• 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: 11/08/2011

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