InjuryMBP

AFT - 1 DIVERTED TUBE

Received Jan 4, 2008 · Event occurred Nov 14, 2007

Report 2249062-2007-00018 · MDR key 974863

Device

Generic name

Bone Void Filler

Manufacturer

Mtf

Catalog number

227005

Product problems

Device remains implanted

Patient

Paralysis
Surgical procedure, additional
Hospitalization required

Narrative

Description of Event or Problem

FOLLOWING TREATMENT OF A VERTEBRAL COMPRESSION FRACTURE, PARALYSIS WAS NOTED AND PT WAS TAKEN BACK INTO THE OPERATING ROOM WITHIN 1 HOUR FOR DECOMPRESSION.