FDA Adverse Event Malfunction Summary report: N

POWER PRO AMBULANCE COT

MDR report key: 6120531 · Received November 22, 2016

Report

Report Number
0001831750-2016-00373
Event Type
Malfunction
Date Received
November 22, 2016
Date of Event
October 31, 2016
Report Date
March 29, 2018
Manufacturer
STRYKER MEDICAL-KALAMAZOO
Product Code
FPO
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AU
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

NO FURTHER INFORMATION WAS OBTAINED ON THE PAIN THE EMT EXPERIENCED.

Additional Manufacturer Narrative · 1

SUPPLEMENTAL SUBMITTED TO INCLUDE UDI.

Description of Event or Problem · 1

IT WAS ALLEGED THAT WHILE LOADING A STRETCHER INTO THE AMBULANCE WITH A PATIENT THE LOADING ARMS WERE ELEVATING TO RAISE THE STRETCHER FROM GROUND LEVEL WHEN THE STRETCHER SLIPPED AND DROPPED ABOUT 20 CM. IT WAS ALLEGED THAT A MEDIC FELT IMMEDIATE PAIN IN THEIR BACK AND NECK AS THE STRETCHER DROPPING PULLED THEM DOWNWARD WHEN IT DROPPED. FURTHER INFORMATION HAS NOT BEEN PROVIDED.

Description of Event or Problem · 1

IT WAS ALLEGED THAT WHILE LOADING A STRETCHER INTO THE AMBULANCE WITH A PATIENT. THE LOADING ARMS WERE ELEVATING TO RAISE THE STRETCHER FROM GROUND LEVEL WHEN THE STRETCHER SLIPPED AND DROPPED ABOUT 20 CM. IT WAS ALLEGED THAT A MEDIC FELT IMMEDIATE PAIN IN THEIR BACK AND NECK AS THE STRETCHER DROPPING PULLED THEM DOWNWARD WHEN IT DROPPED.

Description of Event or Problem · 1

IT WAS ALLEGED THAT WHILE LOADING A STRETCHER INTO THE AMBULANCE WITH A PATIENT. THE LOADING ARMS WERE ELEVATING TO RAISE THE STRETCHER FROM GROUND LEVEL WHEN THE STRETCHER SLIPPED AND DROPPED ABOUT 20 CM. IT WAS ALLEGED THAT A MEDIC FELT IMMEDIATE PAIN IN THEIR BACK AND NECK AS THE STRETCHER DROPPING PULLED THEM DOWNWARD WHEN IT DROPPED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
770950 POWER PRO AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

Patients

Seq Age Sex Outcome Treatment
1