inforMED

GRAFTON PUTTY 10CC

Received Feb 13, 2008

Report 2249062-2008-00003 · MDR key 998864

Device

Generic name

Bone Void Filler

Manufacturer

Osteotech, Inc.

Catalog number

123110

Product problems

  • Insufficient Device Problem Information

Patient

YR

  • Bacterial Infection

Narrative

Description of Event or Problem

THE PATIENT HAD DEVELOPED AN ORGANISM (SERRATIA MARSCENS) AFTER HAVING THE GRAFTS IMPLANTED. THE PATIENT IS TAKING THE AMAKACIN & CEFEPINE.