FDA Adverse Event Injury Summary report: N

PLATE, FIXATION, BONE

MDR report key: 5409846 · Received February 4, 2016

Report

Report Number
2520274-2016-10750
Event Type
Injury
Date Received
February 4, 2016
Report Date
January 15, 2016
Manufacturer
SYNTHES USA
Product Code
HRS
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. VAN HEEST, A.E. AND STROTHMAN, D. (2009). WRIST ARTHRODESIS IN CEREBRAL PALSY. JHS, 34A, 1216-1224. THIS REPORT IS FOR AN UNKNOWN WRIST FUSION PLATE/UNKNOWN QUANTITY/UNKNOWN LOT. (B)(4) REVISION SURGERY. THE INVESTIGATION COULD NOT BE COMPLETED AND NO CONCLUSION COULD BE DRAWN, AS NO DEVICE WAS RETURNED AND NO LOT NUMBER OR PART NUMBER WAS PROVIDED. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Description of Event or Problem · 1

THIS REPORT IS BEING FILED AFTER THE SUBSEQUENT REVIEW OF THE FOLLOWING LITERATURE ARTICLE, VAN HEEST, A.E. AND STROTHMAN, D. (2009). WRIST ARTHRODESIS IN CEREBRAL PALSY. JHS, 34A, 1216-1224. THE AUTHORS CONDUCTED A RETROSPECTIVE REVIEW OF CHARTS AND RADIOGRAPHS TO EXAMINE THE RESULTS OF WRIST ARTHRODESIS USING SYNTHES WRIST FUSION PLATE IN THE TREATMENT OF SKELETALLY MATURE PATIENTS WITH CEREBRAL PALSY FOR SEVERE, FIXED WRIST FLEXION DEFORMITY. RESULTS WERE MEASURED BY FUSION RATE, COMPLICATIONS, AND CLINICAL OUTCOMES. BETWEEN 1995 AND 2007, 34 PATIENTS (41 EXTREMITIES) WITH DEFORMITIES ASSOCIATED WITH CEREBRAL PALSY WERE TREATED BY WRIST ARTHRODESIS USING DORSAL PLATE FIXATION. THE 34 PATIENTS IN THIS STUDY CONSISTED OF 23 MALE AND 11 FEMALE PATIENTS. THE AVERAGE AGE AT THE TIME OF SURGERY WAS 22 YEARS (RANGE, 13-50 YEARS) WITH AVERAGE FOLLOW-UP OF 14 MONTHS (RANGE, 2-70 MONTHS). RESULTS INCLUDED: ONE MALE PATIENT WITH ATHETOID CEREBRAL PALSY TREATED BY WRIST ARTHRODESIS WITHOUT A PROXIMAL ROW CARPECTOMY OR BONE GRAFTING DEVELOPED A NONUNION THAT WAS DIAGNOSED AFTER HARDWARE REMOVAL. HE SUBSEQUENTLY WENT ON TO UNION AFTER REVISION OPEN REDUCTION INTERNAL FIXATION AUGMENTED WITH BONE GRAFT SUBSTITUTE. THIS IS REPORT 1 OF 2 FOR (B)(4). THIS REPORT IS FOR AN UNKNOWN WRIST FUSION PLATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
68435 PLATE, FIXATION, BONE HRS SYNTHES USA

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention