FDA Adverse Event Injury Summary report: N

M2A MAGNUM

MDR report key: 3191026 · Received June 26, 2013

Report

Report Number
0001825034-2013-02267
Event Type
Injury
Date Received
June 26, 2013
Date of Event
December 1, 2007
Report Date
May 30, 2013
Manufacturer
BIOMET ORTHOPEDICS
Product Code
KWA
PMA / PMN Number
PK042037
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. THE FOLLOWING SECTIONS COULD NOT BE COMPLETED WITH THE LIMITED INFORMATION PROVIDED. PRODUCT IDENTIFICATION & EXPIRATION DATE - UNKNOWN. MANUFACTURE DATE ¿ UNKNOWN. THE PRODUCT IDENTIFICATION NECESSARY TO REVIEW MANUFACTURING HISTORY WAS NOT PROVIDED. EVENT IS BEING REPORTED TO FDA ON ONE MEDWATH AS LIMITED INFORMATION IS AVAILABLE. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE COMPLAINT WILL BE REASSESSED AND FURTHER MEDWATCH REPORTS WILL BE SUBMITTED, IF NECESSARY. BIOMET ORTHOPEDICS RECEIVED PRELIMINARY CLINICAL DATA FROM DR. PAUL GROSSO REGARDING PATIENTS ENROLLED IN A MOM CLINICAL STUDY. PLEASE SEE ATTACHED ABSTRACT TITLED ¿PREVALENCE AND PREDICTORS OF PSEUDOTUMOR AND ELEVATED METAL ION LEVELS FOLLOWING LARGE-DIAMETER HEAD METAL-ON-METAL TOTAL HIP ARTHROPLASTY¿.

Description of Event or Problem · 1

BIOMET ORTHOPEDICS RECEIVED PRELIMINARY CLINICAL DATA FROM DR. (B)(6) REGARDING PATIENTS ENROLLED IN A (B)(6) CLINICAL STUDY. IT WAS REPORTED THAT A PATIENT UNDERWENT A LEFT TOTAL HIP ARTHROPLASTY ON (B)(6) 2007. DURING POST OPERATIVE MONITORING AND TESTING FLUID WAS NOTED. THE AREA OF FLUID MEASURED 3.4X2.5X2.0. THESE FINDINGS WERE FOUND DUE TO FOLLOW UP TESTING. NO FURTHER INFORMATION HAS BEEN PROVIDED AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
291040 M2A MAGNUM PROSTHESIS, HIP KWA BIOMET ORTHOPEDICS N/A UNK

Patients

Seq Age Sex Outcome Treatment
1 55 YR Hospitalization