FDA Adverse Event Malfunction Summary report: N

TRANSPORT STRETCHER

MDR report key: 2250900 · Received September 12, 2011

Report

Report Number
3006697241-2011-00103
Event Type
Malfunction
Date Received
September 12, 2011
Date of Event
August 26, 2011
Report Date
August 26, 2011
Manufacturer
HILL-RO DE MEXICO S DE RL DE CV
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE TECH FOUND THE LATCH PLATE HAD A SLIGHT BENT IN IT, CAUSING IT TO RUB AGAINST THE RUBBER ON THE RAIL GUARD. THE LATCH PLATE DIDN'T APPEAR TO HAVE BEEN DAMAGED WHILE IN USE. HE STRAIGHTENED THE LATCH PLATE TO REPAIR THE BED.

Description of Event or Problem · 1

THE ACCOUNT STATED THE SIDERAIL DOES NOT LATCH AUTOMATICALLY. THEY HAVE TO PUSH DOWN ON THE LATCH TO HAVE THE SIDERAIL LATCH PROPERLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRANSPORT STRETCHER WHEELED STRETCHER FPO HILL-RO DE MEXICO S DE RL DE CV 8005

Patients

Seq Age Sex Outcome Treatment
1