FDA Adverse Event Injury Summary report: N

SCREW, FIXATION, BONE

MDR report key: 5539113 · Received March 31, 2016

Report

Report Number
2520274-2016-11886
Event Type
Injury
Date Received
March 31, 2016
Report Date
March 11, 2016
Manufacturer
SYNTHES USA
Product Code
HWC
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE USED FOR TREATMENT, NOT DIAGNOSIS WINKER, K.H. (2005). ¿ANGULAR STABLE PLATE SYSTEMS IN THE DISTAL RADIUS: SOLUTIONS AND PROBLEMS.¿ AKT TRAUMATOL (2005) 35: 151-154. THIS REPORT IS FOR UNKNOWN SCREW, UNKNOWN QUANTITY, UNKNOWN LOT. UDI: UNKNOWN PART NUMBER, UDI IS UNAVAILABLE. (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. 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 JOURNAL ARTICLE, WINKER, K.H. (2005). "ANGULAR STABLE PLATE SYSTEMS IN THE DISTAL RADIUS: SOLUTIONS AND PROBLEMS." AKT TRAUMATOL (2005) 35: 151-154. THE ARTICLE WAS BASED ON A RETROSPECTIVE (YEARS 1996,1997) AND PROSPECTIVE STUDY (1998 AND FORWARD) OF 100 DISTAL RADIUS EXTENSION FRACTURES WHO WERE SURGICALLY TREATED USING ONE OF THREE PLATING SYSTEMS; RADIUS T-PLATE, DISTAL RADIUS PLATE, AND LCP PLATE. THE PURPOSE OF THE STUDY WAS TO DETERMINE THE BENEFITS AND PROBLEMS WITH THE PLATING SYSTEMS. THE FOLLOWING COMPLICATIONS WERE NOTED AS GENERAL COMPLICATIONS NOT ASSOCIATED WITH ANY PARTICULAR PLATE TYPE: TEN (10) INSTANCES OF CORRECTION LOSS; LOSS OF REDUCTION POST-OPERATIVELY. THIS IS REPORT 1 OF 2 FOR (B)(4). THIS REPORT IS FOR UNKNOWN SCREWS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
192980 SCREW, FIXATION, BONE HWC SYNTHES USA

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention