FDA Adverse Event Injury Summary report: N

APEX ARC HIP STEM

MDR report key: 4397888 · Received January 4, 2015

Report

Report Number
MW5040040
Event Type
Injury
Date Received
January 4, 2015
Date of Event
February 20, 2012
Report Date
January 4, 2014
Manufacturer
OMNI LIFE SCIENCE
Product Code
LZO
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
FL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

PATIENT HAD A LEFT TOTAL HIP ARTHROPLASTY ON (B)(6) 2012 FOR ADVANCED OSTEOARTHRITIS. THERE WERE NO COMPLICATIONS WITH THE SURGERY AND THE PT DID WELL FOR ELEVEN MONTHS. SHE COMPLAINED OF SWELLING OF THE WHOLE LEFT LOWER EXTREMITY AND A MASS MEDIALLY. AFTER MANY TESTS, A PSEUDOTUMOR CONSISTING OF NECROTIC TISSUE WAS FOUND. SHE UNDERWENT A LAPAROSCOPIC RESECTION OF THE LEFT RETROPERITONEAL TUMOR AND A REVISION LEFT TOTAL HIP ARTHROPLASTY WITH DEBUNKING OF THE PSEUDOTUMOR SEVEN DAYS LATER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1627 APEX ARC HIP STEM HIP PROSTHESIS, UNCEMENTED LZO OMNI LIFE SCIENCE HC-21003-HA 8629

Patients

Seq Age Sex Outcome Treatment
1 68 YR Hospitalization| R