FDA Adverse Event Malfunction Summary report: N

PROCEDURAL STRETCHER

MDR report key: 1946057 · Received December 10, 2010

Report

Report Number
3006697241-2010-00055
Event Type
Malfunction
Date Received
December 10, 2010
Date of Event
November 16, 2010
Report Date
November 16, 2010
Manufacturer
HILL-ROM DE MEXICO S DE RL DE CV
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH ADJUSTED ALL FOUR CASTERS TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFO RECEIVED INDICATES THE CASTERS ROLL SLIGHTLY WHEN IN BRAKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8000

Patients

Seq Age Sex Outcome Treatment
1