inforMED
InjuryHQH

MEDPOR SPHERE

Received Jan 27, 2005 · Event occurred Jun 23, 2004

Report 1057129-2005-00005 · MDR key 568949

Device

Generic name

Artificial Eye

Manufacturer

Porex Surgical

Model number

UNK

Catalog number

UNK

Lot number

UNK

Product problems

  • Explanted

Patient

UNKNOWN

  • Bleeding
  • Discomfort
  • Surgical procedure

Narrative

Description of Event or Problem

EMAIL FROM PT WHO RECEIVED AN ARTIFICIAL EYE MADE OF MEDPOR MATERIAL IN 1996. PT WAS EXPERIENCING UNCOMFORTABLE FEELING WITH BLOOD IN TEARS. IMPLANT WAS REMOVED IN AUGUST 2004. PT WAS CONTACTED AND HAD THE IMPLANT REMOVED AND WAS FEELING WELL, BUT DID NOT PROVIDE OTHER INFO. PRODUCT WAS NOT RETURNED.