FDA Adverse Event Malfunction Summary report: N

30" TRANSPORT STRETCHER

MDR report key: 1021036 · Received March 28, 2008

Report

Report Number
1831750-2008-00037
Event Type
Malfunction
Date Received
March 28, 2008
Date of Event
March 13, 2008
Report Date
March 13, 2008
Manufacturer
STRYKER CORP., MEDICAL DIV.
Product Code
FPO
Removal / Correction Number
RECALL Z-219/239-08
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE BRAKES WERE NOT WORKING PROPERLY. NO INJURY TO THE PT OR CAREGIVER WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 30" TRANSPORT STRETCHER STRETCHER FPO STRYKER CORP., MEDICAL DIV. 1004 NA

Patients

Seq Age Sex Outcome Treatment
1 UNK Required Intervention