FDA Adverse Event Malfunction Summary report: N

VA-LCP-2-COLUMN DRP2.4 VOLAR NARR LE SHA

MDR report key: 3132071 · Received May 29, 2013

Report

Report Number
8030965-2013-02447
Event Type
Malfunction
Date Received
May 29, 2013
Date of Event
April 25, 2013
Report Date
April 30, 2013
Manufacturer
SYNTHES GMBH
Product Code
HWC
PMA / PMN Number
K092556
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS DEVICE USED FOR TREATMENT AND NOT DIAGNOSIS. ADD'L PRO CODE: HRS. THE MANUFACTURING RECORDS WERE REVIEWED AND NO COMPLAINT RELATED ISSUES WERE FOUND. NO PRODUCT WAS RETURNED FOR FURTHER INVESTIGATION.

Description of Event or Problem · 1

A DEVICE REPORT FROM SYNTHES (B)(4) INDICATED A SURGEON IN (B)(6) REPORTED: DURING SURGERY FOR A DISTAL RADIUS FRACTURE, THE SURGEON INSERTED AND LOCKED 4 VA LOCKING SCREWS IN DISTAL HOLES BY GUIDING BLOCK, AND FIXED BY DRIVER WITH TORQUE LIMITER. SECOND, HE INSERTED AND LOCKED 2.7MM 2 CORT.SCREWS IN PROXIMAL SHAFT HOLES BY DRIVER WITH TORQUE LIMITER. THIRD, HE INSERTED AND LOCKED 2.7MM 2 VA LOCKING SCREWS IN PROXIMAL VA HOLES BY TORQUE LIMITER, BY THIS TIME, ALL SCREWS COULD BE LOCKED. AND THEN HE TOOK OFF GUIDING BLOCK FIXED VA LOCKING SCREWS BY DRIVE WITH TORQUE LIMITER JUST IN CASE. HOWEVER, VA LOCKING SCREW IN DISTAL ROW MOST STYLOID SIDE HAD NOT STOPPED ROTATION. FINALLY THIS SCREW WAS PENETRATED IN HOLE. HE FOUND A METAL PART LIKE THREAD WHICH WAS ADHERED IN THE PATIENT BODY. SURGERY WAS PERFORMED BY GLOBAL TECHNICAL METHOD. HE CHOSE FIXED MODE, AND USED TORQUE LIMITER 0.8NM IN LOCK. THE METAL CHIP IS BEING RETURNED. THIS IS 3 OF 3 REPORTS FOR COMPLAINT (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
236401 VA-LCP-2-COLUMN DRP2.4 VOLAR NARR LE SHA HWC SYNTHES GMBH 8205753

Patients

Seq Age Sex Outcome Treatment
1 65 YR