inforMED
InjuryKGS

SDI

Received Mar 8, 1999

Report 1219161-1999-00192 · MDR key 213218

Device

Generic name

Unk

Model number

NA

Catalog number

UNK

Lot number

UNK

Product problems

  • Explanted
  • Device Issue

Patient

UNKNOWN

  • Pain
  • Surgical procedure, repeated
  • Surgical procedure

Narrative

Description of Event or Problem

THE DEVICE WAS USED DURING A TFC FUSION CAGE EXPLANTATION. REPORTEDLY, ONE CAGE WAS EXPLANTED BECAUSE THE PT WAS EXPERIENCING LEG PAIN. THE HOSP HAS REPORTED THE PT'S CONDITION IS SATISFACTORY.