FDA Adverse Event Malfunction Summary report: N

EPIC II CRITICAL CARE BED

MDR report key: 2222507 · Received July 13, 2011

Report

Report Number
1831750-2011-07028
Event Type
Malfunction
Date Received
July 13, 2011
Date of Event
June 16, 2011
Report Date
June 16, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Removal / Correction Number
Z-2586-2010
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

CONCLUSION: FOWLER BEARING SUPPORT, FOWLER WELDMENT BOX.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER WAS STUCK AND COULD NOT BE LOWERED. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EPIC II CRITICAL CARE BED A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 2030 EPIC+ NA

Patients

Seq Age Sex Outcome Treatment
1