InjuryLPQ
EXOGEN
Received Apr 3, 2012 · Event occurred Apr 3, 2012
Report 1020279-2012-00210 · MDR key 2515175
Device
Generic name
4000+ System
Manufacturer
Smith & Nephew Orthopaedics, Inc.Catalog number
71034100
Lot number
11FM02549
Product problems
- Insufficient Device Problem Information
Patient
Not reported
- No Code Available
Narrative
Description of Event or Problem
IT WAS REPORTED THAT PATIENT'S X-RAYS INDICATE THAT PAROSTEAL OSTEOSARCOMA OF THE RIGHT PROXIMAL HUMERUS HAS RETURNED.
Description of Event or Problem
IT WAS INITIALLY REPORTED THAT PATIENT'S X-RAY INDICATED PAROSTEAL OSTEOSARCOMA OF THE RIGHT HUMEUS HAS RETURNED, WHICH THE TREATING PHYSICIAN REPORTED THERE WAS NO CASUAL RELATIONSHIP TO THE USE OF THE EXOGEN DEVICE.