FDA Adverse Event Injury Summary report: N

M2A MAGNUM PF CUP 54MM O.D. X 48MM I.D.

MDR report key: 5901672 · Received August 24, 2016

Report

Report Number
0001825034-2016-03230
Event Type
Injury
Date Received
August 24, 2016
Date of Event
April 3, 2015
Report Date
July 25, 2016
Manufacturer
BIOMET ORTHOPEDICS
Product Code
KWA
PMA / PMN Number
PK042037
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KY, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

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 POSSIBLE ADVERSE EFFECTS, NUMBER 8 STATES, "DISLOCATION AND SUBLUXATION DUE TO INADEQUATE FIXATION, MALALIGNMENT, MALPOSITION, EXCESSIVE, UNUSUAL AND/OR AWKWARD MOVEMENT AND/OR ACTIVITY, TRAUMA, WEIGHT GAIN, OR OBESITY. MUSCLE AND FIBROUS TISSUE LAXITY CAN ALSO CONTRIBUTE TO THESE CONDITIONS. " THIS REPORT IS NUMBER 4 OF 4 MDRS FILED FOR THE SAME PATIENT (REFERENCE 1825034-2015-04804, 2016-03202 & 03225 & 03230). REMAINS IMPLANTED.

Additional Manufacturer Narrative · 1

CONCOMITANT MEDICAL PRODUCTS: BIOMET CERAMIC TAPER ADAPTER, CATALOG#: 650-1067, LOT#: 080270; BIOMET FEMORAL STEM, CATALOG#: 192410, LOT#: 347410.

Description of Event or Problem · 1

PATIENT UNDERWENT A RIGHT HIP REVISION PROCEDURE APPROXIMATELY TWO MONTHS POST-IMPLANTATION DUE TO DISLOCATION AND DISASSOCIATION OF THE POLY BEARING FROM THE HEAD. THE CERAMIC HEAD AND HIP BEARING WERE REMOVED AND REPLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
553583 M2A MAGNUM PF CUP 54MM O.D. X 48MM I.D. PROSTHESIS, HIP KWA BIOMET ORTHOPEDICS N/A 031180

Patients

Seq Age Sex Outcome Treatment
1 40 YR Hospitalization| R