FDA Adverse Event Malfunction Summary report: N

HEAD/NECK SURG BED

MDR report key: 2081759 · Received April 13, 2011

Report

Report Number
1831750-2011-03520
Event Type
Malfunction
Date Received
April 13, 2011
Date of Event
March 15, 2011
Report Date
March 15, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE BLACK PART OF THE CASTER IS PEELING OFF. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HEAD/NECK SURG BED HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0966 NA

Patients

Seq Age Sex Outcome Treatment
1 NA