FDA Adverse Event Malfunction Summary report: N

BASIC CONFIGURATION MODEL 6100 BASE

MDR report key: 2070353 · Received April 18, 2011

Report

Report Number
1831750-2011-03704
Event Type
Malfunction
Date Received
April 18, 2011
Date of Event
March 22, 2011
Report Date
March 22, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION UNDERWAY.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE COT SLID DOWN AT THE HEAD END. THERE WAS REPORTED PT INVOLVEMENT HOWEVER THERE HAVE BEEN NO REPORTED ADVERSE CONSEQUENCES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BASIC CONFIGURATION MODEL 6100 BASE STRETCHER, WHEELED FPO STRYKER MEDICAL 6100 NA

Patients

Seq Age Sex Outcome Treatment
1