FDA Adverse Event Malfunction Summary report: N

PROCEDURAL STRETCHER

MDR report key: 2243457 · Received August 29, 2011

Report

Report Number
3006697241-2011-00093
Event Type
Malfunction
Date Received
August 29, 2011
Date of Event
August 16, 2011
Report Date
August 16, 2011
Manufacturer
HILL-ROM DE MEXICO S DE RL DE CV
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECH ADJUSTED THE BRAKE LINKAGE AT THE HEAD END AND THE BRAKE POSITION ON BOTH FOOT END CASTERS TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFO RECEIVED INDICATES, THE BRAKE IS NOT HOLDING.

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