FDA Adverse Event Malfunction Summary report: N

EYE SURGERY STRETCHER

MDR report key: 1760128 · Received July 12, 2010

Report

Report Number
1831750-2010-01511
Event Type
Malfunction
Date Received
July 12, 2010
Date of Event
June 23, 2010
Report Date
June 23, 2010
Manufacturer
STRYKER CORP., MEDICAL DIV.
Product Code
FPO
Removal / Correction Number
Z-0281-2010
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THE FOWLER IS STUCK IN A DOWN POSITION AND CANNOT BE RAISED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EYE SURGERY STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV. 1079

Patients

Seq Age Sex Outcome Treatment
1 NA