FDA Adverse Event Injury Summary report: N

SCREW,FIXATION, SCREW

MDR report key: 4636145 · Received March 26, 2015

Report

Report Number
2520274-2015-12240
Event Type
Injury
Date Received
March 26, 2015
Report Date
February 27, 2014
Manufacturer
SYNTHES USA
Product Code
HWC
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS DEVICE IS USE FOR TREATMENT NOT DIAGNOSIS (B)(4). THIS IS FOR AN UNKNOWN SCREW, UNKNOWN LOT OR PART NUMBER. 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 LONG TERM RESULTS OF RECONSTRUCTION PLATES IN LATERAL MANDIBULAR DEFECTS REVISION OF NINE CASESJ. ARIAS-GALLO ET AL. / AURIS NASUS LARYNX 31 (2004) 57¿63. THIS ARTICLE ORIGIN IS (B)(4). THE CLINICAL RECORDS OF NINE PATIENTS, SEVEN MEN AND TWO WOMEN, AGED 56¿73 YEARS WERE REVIEWED. THE RECORDS OF NINE CANCER PATIENTS WHO UNDERWENT LATERAL MANDIBULAR RESECTIONS (WITH PRESERVATION OF BOTH CONDYLE AND SYMPHYSIS) FOLLOWED BY RECONSTRUCTION WITH A MANDIBULAR RECONSTRUCTION PLATE,WERE RETROSPECTIVELY REVIEWED. PATIENTS WERE TREATED BETWEEN 1991 AND 1995 WITH REGULAR SYNTHES AND LEIBINGER PLATES (WITHOUT LOCKING SCREWS). FOLLOW RANGED FROM 5 TO 11 YEARS POST IMPLANT. EIGHT PATIENTS HAD SQUAMOUS CELL CARCINOMA AND ONE PATIENT HAD CLEAR CELL ODONTOGENIC CARCINOMA. ALL THE PATIENTS WERE TREATED WITH LOCAL AND REGIONAL SURGERY WITHOUT ABLATION OF EITHER THE CONDYLE OR THE SYMPHYSIS, A TYPE L RESECTION IN BOYD CLASSIFICATION [7], AND RECONSTRUCTED BY MEANS OF A MANDIBULAR RECONSTRUCTION PLATE. PATIENT 4 A (B)(6) HAD PROXIMAL SCREW LOOSENING THIS IS REPORT 2 OF 8 FOR (B)(4). THIS REPORT IS FOR A UNKNOWN SCREW.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
204026 SCREW,FIXATION, SCREW HWC SYNTHES USA

Patients

Seq Age Sex Outcome Treatment
1 73 YR