FDA Adverse Event Malfunction Summary report: N

POWER PRO AMBULANCE COT

MDR report key: 2140777 · Received June 15, 2011

Report

Report Number
1831750-2011-05972
Event Type
Malfunction
Date Received
June 15, 2011
Date of Event
June 5, 2011
Report Date
June 5, 2011
Manufacturer
STRYKER MEDICAL
Product Code
INK
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

OTHER: CASTER HORNS.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE COT HAD BENT CASTER HORNS. THERE WAS PT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 POWER PRO AMBULANCE COT STRETCHER, WHEELED INK STRYKER MEDICAL 6500 NA

Patients

Seq Age Sex Outcome Treatment
1