InjuryLFF
SYNCHROMED II
Received May 8, 2007 · Event occurred Mar 1, 2007
Report 2182207-2007-01585 · MDR key 846997
Device
Generic name
Lkk
Manufacturer
Medtronic, Inc. Neurological Div.Model number
863720Catalog number
NA
Lot number
NA
Product problems
- Unknown (for use when the device problem is not known)
Patient
69 YR
- Therapeutic Response, Decreased
Narrative
Description of Event or Problem
THE MFR'S REP REPORTED THE PT WAS EXPERIENCING A DECREASE IN THEIR PAIN THERAPY. THE HCP PERFORMED A ROTOR STUDY, BUT WANTED THE RESULTS REVIEWED BY THE MFR. A FOLLOW-UP REPORT WILL BE SENT ONCE THE ROTOR STUDY IS REVIEWED BY THE MFR. NO PT INJURY WAS REPORTED. THE PT'S FINAL OUTCOME IS UNK. THE DRUG CONTAINED IN THE PT'S PUMP IS UNK. ADD'L INFO HAS BEEN REQUESTED, BUT WAS NOT AVAILABLE AT THE TIME OF THIS REPORT.