FDA Adverse Event Malfunction Summary report: N

GOBED II MED/SURG BED

MDR report key: 2141428 · Received June 1, 2011

Report

Report Number
1831750-2011-05371
Event Type
Malfunction
Date Received
June 1, 2011
Date of Event
May 5, 2011
Report Date
May 5, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FNL
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WV, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

TRANSPORTING ACCIDENT BY CUSTOMER.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE CASTINGS FROM THE HEAD RIGHT SIDE RAIL WERE BROKEN OFF AND THERE WERE SHARP EDGES. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 GOBED II MED/SURG BED A/C HOSPITAL BED FNL STRYKER MEDICAL FL28C NA

Patients

Seq Age Sex Outcome Treatment
1 UNK