FDA Adverse Event Injury Summary report: N

M2A-MAGNUM 42-50M TPR INSRT +3

MDR report key: 6733180 · Received July 21, 2017

Report

Report Number
0001825034-2017-05112
Event Type
Injury
Date Received
July 21, 2017
Report Date
September 8, 2017
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
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DESIGN HISTORY RECORDS WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. REVIEW OF THE COMPLAINT HISTORY DETERMINED THAT NO FURTHER ACTION IS REQUIRED AS NO WERE TRENDS IDENTIFIED. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

Additional Manufacturer Narrative · 1

THE COMPLAINT NUMBER CORRESPONDING TO THIS MEDWATCH IS (B)(4). IT IS UNKNOWN IF THE DEVICE WILL BE RETURNED FOR ANALYSIS; HOWEVER, AN INVESTIGATION OF THE REPORTED EVENT IS IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETED, A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED. (B)(6). CONCOMITANT MEDICAL PRODUCTS - UNKNOWN CUP, UNKNOWN STEM, 139258 M2A MAGNUM TPR INSRT 103680 & 157446 M2A MAGNUM MOD HD 323240.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO CORROSION AND ELEVATED ION LEVELS CAUSING BONE DISSOLUTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
512901 M2A-MAGNUM 42-50M TPR INSRT +3 PROSTHESIS, HIP KWA BIOMET ORTHOPEDICS N/A 103680

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R