InjuryKGS
SDI
Received Mar 8, 1999
Report 1219161-1999-00183 · MDR key 213185
Device
Generic name
Unk
Manufacturer
United States Surgical CorporationModel number
NACatalog number
UNK
Lot number
UNK
Product problems
- Explanted
- Device Issue
Patient
UNKNOWN
- Surgical procedure, repeated
- Surgical procedure
Narrative
Description of Event or Problem
THE DEVICE WAS USED DURING A TFC FUSION CAGE EXPLANTATION. REPORTEDLY, THE CAGES WERE EXPLANTED FROM THE PT DUE TO UNSPECIFIED REASONS. THE HOSP HAS REPORTED THE PT'S CONDITION IS SATISFACTORY.