FDA Adverse Event Injury Summary report: N

PLATE, FIXATION, BONE

MDR report key: 6537126 · Received May 2, 2017

Report

Report Number
2520274-2017-11566
Event Type
Injury
Date Received
May 2, 2017
Report Date
April 5, 2017
Manufacturer
SYNTHES (USA)
Product Code
HRS
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. PATIENT INFORMATION IS NOT AVAILABLE FOR REPORTING. PARK, K.S., CHAN, C.K., LEE, G.W., AHN, H.W., AND YOON, T.R. (2017) OUTCOME OF ALTERNATIVE APPROACH TO DISPLACED ACETABULAR FRACTURES. INJURY, INT. J. CARE INJURED 48(2017)388-393. SOUTH KOREA. THIS IS FOR UNKNOWN PLATE/UNKNOWN PART NUMBER/UNKNOWN LOT. (UDI): UNKNOWN PART NUMBER, UDI IS UNAVAILABLE. THE SUBJECT DEVICE IS NOT EXPECTED TO BE RETURNED TO THE SYNTHES MANUFACTURER FOR EVALUATION. WITHOUT A LOT NUMBER THE DEVICE HISTORY RECORDS REVIEW COULD NOT BE COMPLETED. THE INVESTIGATION COULD NOT BE COMPLETED; NO CONCLUSION COULD BE DRAWN, AS NO PRODUCT WAS RECEIVED. (B)(4). 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

LITERATURE ARTICLE RECEIVED. THIS REPORT IS BEING FILED AFTER THE SUBSEQUENT REVIEW OF THE FOLLOWING LITERATURE ARTICLE: PARK, K.S., CHAN, C.K., LEE, G.W., AHN, H.W., AND YOON, T.R. (2017) OUTCOME OF ALTERNATIVE APPROACH TO DISPLACED ACETABULAR FRACTURES. INJURY, INT. J. CARE INJURED 48(2017)388-393. SOUTH KOREA. A RETROSPECTIVE STUDY WAS CARRIED OUT WITH 23 PATIENTS (17 MALES, 6 FEMALES) WITH AN AVERAGE AGE OF 50.1 YEARS (RANGE, 36-68 YEARS) WITH DISPLACED ACETABULAR FRACTURE TREATED WITH COMBINED INCISION AND PLATE-CABLE SYSTEMS. THE MEAN BODY MASS INDEX WAS 21.3 (RANGE, 15.8-27.7). A CURVED RECONSTRUCTION PLATE (SYNTHES, PAOLI, PA) WAS USED AFTER THE CABLE REDUCTION. THERE WERE 12 ANATOMICAL, 6 IMPERFECT, AND 5 POOR REDUCTIONS. COMPLICATIONS DOCUMENTED: A (B)(6) MALE PATIENT EXPERIENCED NONUNION AND PAINFUL LIMPING REQUIRING REVISION SURGERY (CONVERSION TO TOTAL HIP ARTHROPLASTY). THIS IS REPORT 2 OF 2 FOR (B)(4). THIS REPORT IS FOR AN UNKNOWN SYNTHES RECONSTRUCTION PLATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
318275 PLATE, FIXATION, BONE HRS SYNTHES (USA)

Patients

Seq Age Sex Outcome Treatment
1 64 YR Required Intervention