FDA Adverse Event Malfunction Summary report: N

MX-PRO AMBULANCE COT

MDR report key: 2243155 · Received August 31, 2011

Report

Report Number
1831750-2011-09358
Event Type
Malfunction
Date Received
August 31, 2011
Date of Event
August 3, 2011
Report Date
August 3, 2011
Manufacturer
STRYKER MEDICAL
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

O2 BOTTLE HOLDER.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE O2 BOTTLE HOLDER WAS BROKEN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MX-PRO AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL 6080 NA

Patients

Seq Age Sex Outcome Treatment
1