FDA Adverse Event Malfunction Summary report: N

ADVANTAGE SERIES 26

MDR report key: 1940382 · Received December 9, 2010

Report

Report Number
1831750-2010-04686
Event Type
Malfunction
Date Received
December 9, 2010
Date of Event
November 12, 2010
Report Date
November 12, 2010
Manufacturer
STRYKER CORP., MEDICAL DIV.
Product Code
FPO
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

IV POLE ASSEMBLY.

Description of Event or Problem · 1

IT WAS REPORTED BY SERVICE REPORT THAT THE IV POLE SNAPPED OFF AT THE TOP THREADED PORTION OF THE MIDDLE STAGE. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ADVANTAGE SERIES 26 HOSPITAL WHEELED STRETCHER FPO STRYKER CORP., MEDICAL DIV. 1001 NA

Patients

Seq Age Sex Outcome Treatment
1