FDA Adverse Event Malfunction Summary report: N

OBGYN STRETCHER

MDR report key: 2083381 · Received April 29, 2011

Report

Report Number
3006697241-2011-00034
Event Type
Malfunction
Date Received
April 29, 2011
Date of Event
April 5, 2011
Report Date
April 5, 2011
Manufacturer
HILL-ROM DE MEXICO S DE RL DE CV
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NM, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE TECHNICIAN FOUND THE BRAKE/STEER LINKAGE WAS DISCONNECTED. HE RECONNECTED THE LINKAGE TO REPAIR THE STRETCHER.

Description of Event or Problem · 1

INFORMATION RECEIVED INDICATES THE BRAKES WOULD SET AT ONE END OF THE STRETCHER, BUT NOT HOLD AT THE OTHER END.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 OBGYN STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8050

Patients

Seq Age Sex Outcome Treatment
1