FDA Adverse Event Malfunction Summary report: N

ST104 TRANSPORT

MDR report key: 3070669 · Received April 22, 2013

Report

Report Number
0001831750-2013-03592
Event Type
Malfunction
Date Received
April 22, 2013
Date of Event
March 25, 2013
Report Date
March 25, 2013
Manufacturer
STRYKER MEDICAL-KALAMAZOO
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
HK
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE IV POLE HAS SHARP EDGES EXPOSED. MANUFACTURER'S INVESTIGATION IS ONGOING. IF ADDITIONAL INFORMATION IS RECEIVED, A FOLLOW-UP REPORT MAY BE SUBMITTED. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
171520 ST104 TRANSPORT STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

Patients

Seq Age Sex Outcome Treatment
1