FDA Adverse Event Summary report: N

POWER PRO AMBULANCE COT

MDR report key: 1240805 · Received November 14, 2008

Report

Report Number
1831750-2008-00162
Date Received
November 14, 2008
Date of Event
October 29, 2008
Report Date
October 24, 2008
Manufacturer
STRYKER CORP. MEDICAL DIVISION
Product Code
FPO
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE SAFETY HOOK WAS NOT INSTALLED CORRECTLY BY THE CUSTOMER. THE HOOK WAS INSTALLED IN SUCH A WAY THAT THE COT COULD GO AROUND IT WHEN REMOVING FROM THE AMBULANCE.

Description of Event or Problem · 1

IT WAS REPORTED THAT A COT DROPPED WHEN UNLOADING FROM THE AMBULANCE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 POWER PRO AMBULANCE COT AMBULANCE COT FPO STRYKER CORP. MEDICAL DIVISION 6500 NOT APPLICABLE

Patients

Seq Age Sex Outcome Treatment
1 UNK