FDA Adverse Event Other Summary report: N

UNKNOWN

MDR report key: 2121974 · Received June 3, 2011

Report

Report Number
1831750-2011-05479
Event Type
Other
Date Received
June 3, 2011
Date of Event
May 6, 2011
Report Date
May 6, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE USER FACILITY WAS UNABLE TO IDENTIFY THE STRETCHER MODEL/SERIAL NUMBER IN USE AT THE TIME OF THIS EVENT. THE 10-12 STRETCHERS WERE INSPECTED. CODING REFLECTS THE EVAL FINDINGS FOR THESE STRETCHERS. IF ANY FURTHER INFO IS OBTAINED RELATED TO THIS EVENT, A F/U MEDWATCH REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT HAS BEEN REPORTED BY THE USER FACILITY THAT A MATTRESS SLID OFF OF A STRETCHER RESULTING IN A PT FALL. IT WAS REPORTED THAT THERE WAS NO INJURY TO THE PT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNKNOWN HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL UNK NA

Patients

Seq Age Sex Outcome Treatment
1