FDA Adverse Event Malfunction Summary report: N

SECURE 3 MED/SURG BED

MDR report key: 1942725 · Received December 10, 2010

Report

Report Number
1831750-2010-04717
Event Type
Malfunction
Date Received
December 10, 2010
Date of Event
November 16, 2010
Report Date
November 16, 2010
Manufacturer
STRYKER CORP., MEDICAL DIV.
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CONCLUSIONS: DIP SWITCHES SET CORRECTLY FOR HOSPITAL NURSE CALL SYSTEM.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE NURSE CALL DOESN'T WORK. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SECURE 3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 3002S3 NA

Patients

Seq Age Sex Outcome Treatment
1