FDA Adverse Event Death Summary report: N

UNIDRIVE GYN MORCELLATOR MOTOR SYSTEM

MDR report key: 5808874 · Received July 20, 2016

Report

Report Number
9610617-2016-00114
Event Type
Death
Date Received
July 20, 2016
Date of Event
October 18, 2012
Report Date
July 20, 2016
Manufacturer
KARL STORZ GMBH & CO. KG TUTTLINGEN, GERMANY
Product Code
GCJ
PMA / PMN Number
K061180
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
DC, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

THERE WAS NO INDICATION OF ANY MALFUNCTION OF THE DEVICE. THE DEVICE WAS NOT RETURNED.

Description of Event or Problem · 1

ALLEGEDLY, THE PATIENT UNDERWENT A LAPAROSCOPIC HYSTERECTOMY FOR THE TREATMENT OF UTERINE FIBROID(S) AND WAS DIAGNOSED WITH EPITHELIOID LEIOMYOSARCOMA SHORTLY AFTER HER SURGERY, BASED ON THE PATHOLOGICAL ANALYSIS. SHE DIED ON (B)(6) 2015.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
462814 UNIDRIVE GYN MORCELLATOR MOTOR SYSTEM MORCELLATOR GCJ KARL STORZ GMBH & CO. KG TUTTLINGEN, GERMANY 26711101-1

Patients

Seq Age Sex Outcome Treatment
1 Death