FDA Adverse Event Injury Summary report: N

PLATE, FIXATION, BONE

MDR report key: 5007543 · Received August 17, 2015

Report

Report Number
2520274-2015-15242
Event Type
Injury
Date Received
August 17, 2015
Report Date
August 4, 2015
Manufacturer
SYNTHES USA
Product Code
HRS
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

ANDRADE-SILVA, F.B., MD, PHD, KOJIMA, K.E., MD, PHD, JOERIS, A., MD, SILVA, J.S., MD, PHD, AND MATTAR JR., R., MD, PHD (2015). SINGLE, SUPERIORLY PLACED RECONSTRUCTION PLATE COMPARED WITH FLEXIBLE INTRAMEDULLARY NAILING FOR MIDSHAFT CLAVICULAR FRACTURES. J BONE JOINT SURG AM. 97(8), 620-626. THIS REPORT IS FOR AN UNKNOWN PLATE. (B)(4) 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. DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. 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 SUBSEQUENT REVIEW OF THE FOLLOWING JOURNAL ARTICLE, ANDRADE-SILVA, F.B., MD, PHD, KOJIMA, K.E., MD, PHD, JOERIS, A., MD, SILVA, J.S., MD, PHD, AND MATTAR JR., R., MD, PHD (2015). SINGLE, SUPERIORLY PLACED RECONSTRUCTION PLATE COMPARED WITH FLEXIBLE INTRAMEDULLARY NAILING FOR MIDSHAFT CLAVICULAR FRACTURES. J BONE JOINT SURG AM. 97(8), 620-626. IN THIS PROSPECTIVE, RANDOMIZED CONTROLLED TRIAL, FIFTY-NINE PATIENTS WITH DISPLACED MIDSHAFT CLAVICULAR FRACTURES WERE RANDOMLY ASSIGNED (BETWEEN MAY 2010 AND JANUARY 2013) TO RECEIVE FIXATION WITH EITHER A RECONSTRUCTION PLATE (THIRTY-THREE PATIENTS), KNOWN AS THE PLATE GROUP, OR ELASTIC STABLE INTRAMEDULLARY NAILING (ESIN; TWENTY-SIX PATIENTS), KNOWN AS THE NAIL GROUP. IN THE PLATE GROUP, THE FRACTURE WAS FIXED USING A SYNTHES 3.5-MM NON-LOCKED RECONSTRUCTION PLATE. IN THE NAIL GROUP, ONE SYNTHES TITANIUM ELASTIC NAIL [TEN] WAS INSERTED PER FRACTURE THROUGH THE MEDIAL FRAGMENT. THE NAIL DIAMETERS WERE 2.0, 2.5, OR 3.0 MM. ELEVEN PATIENTS IN THE PLATE GROUP (38%) PRESENTED WITH IMPLANT BENDING (WITH GREATER CLAVICULAR SHORTENING DUE TO THE BENDING DEFORMITY AT THE FRACTURE SITE). THIS REPORT IS FOR AN UNKNOWN PLATE. THIS IS REPORT 5 OF 6 FOR (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
542151 PLATE, FIXATION, BONE HRS SYNTHES USA

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention