FDA Adverse Event Malfunction Summary report: N

SECURE 3 MED/SURG BED

MDR report key: 1940427 · Received December 9, 2010

Report

Report Number
1831750-2010-04679
Event Type
Malfunction
Date Received
December 9, 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
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

RESULT: FOWLER CLUTCH/BRAKE.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER WOULD NOT FULLY SUPPORT WEIGHT, WOULD SLOWLY LOWER WHEN WEIGHT WAS APPLIED. NO PT 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