FDA Adverse Event Injury Summary report: N

M2A 38MM NON-FLARED ONE PIECE CUP 38MM X 50 O.D.

MDR report key: 1871742 · Received October 15, 2010

Report

Report Number
1825034-2010-00424
Event Type
Injury
Date Received
October 15, 2010
Date of Event
April 10, 2008
Report Date
September 22, 2010
Manufacturer
BIOMET ORTHOPEDICS
Product Code
KWA
PMA / PMN Number
K011110
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

DURING A SURGEON CONFERENCE PRESENTATION, REVISION PROCEDURES RELATED TO BIOMET PRODUCT WERE BEING DISCUSSED. SUBSEQUENTLY, BIOMET CONTACTED THE SURGEON'S OFFICE TO OBTAIN MORE DETAILED INFORMATION REGARDING THE EVENTS DISCUSSED DURING THE CONFERENCE. IT WAS CONFIRMED THAT BIOMET HAD NOT BEEN NOTIFIED OF THE EVENTS AND INFORMATION WAS SUPPLIED TO BIOMET ON (B)(6) 2010. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. REVIEW OF DEVICE HISTORY RECORDS SHOW THAT LOT RELEASED WITH NO RECORDED ANOMALY OR DEVIATION. THERE ARE WARNINGS IN THE PACKAGE INSERT THAT STATE THAT THIS TYPE OF EVENT CAN OCCUR: UNDER "WARNINGS", IT STATES, "IMPROPER SELECTION, PLACEMENT, POSITIONING, ALIGNMENT AND FIXATION OF THE IMPLANT COMPONENTS MAY RESULT IN UNUSUAL STRESS CONDITIONS WHICH MAY LEAD TO SUBSEQUENT REDUCTION IN THE SERVICE LIFE OF THE PROSTHETIC COMPONENTS." THIS REPORT SUBMITTED (B)(6) 2010.

Description of Event or Problem · 1

IT WAS REPORTED THAT PATIENT UNDERWENT TOTAL HIP ARTHROPLASTY ON (B)(6) 2004. SUBSEQUENTLY, PATIENT WAS REVISED ON (B)(6) 2008, DUE TO LOOSENING OF THE ACETABULAR CUP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 M2A 38MM NON-FLARED ONE PIECE CUP 38MM X 50 O.D. PROSTHESIS, HIP KWA BIOMET ORTHOPEDICS N/A 270690

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R