FDA Adverse Event Injury Summary report: N

EXPLOR 2X26MM IMPLANT STEM WITH SCREW

MDR report key: 6533470 · Received May 1, 2017

Report

Report Number
0001825034-2017-02735
Event Type
Injury
Date Received
May 1, 2017
Report Date
May 1, 2017
Manufacturer
BIOMET ORTHOPEDICS
Product Code
KWI
PMA / PMN Number
PK040611
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(6). CONCOMITANT MEDICAL PRODUCT: EXPLOR 10X22 RADIAL HEAD, CAT#: 11-210031, LOT#: NI. INITIAL REPORTER - THE ARTICLE WAS WRITTEN BY SCHUYLER J HALVERSON, MIHIR J DESAI AND DONALD H LEE. HALVERSON ET AL. "CLINICAL OUTCOMES OF BIOMET EXPLOR MODULAR RADIAL HEAD ARTHROPLASTY SYSTEM" JOURNAL TITLE. 37:853-858. REPORTED EVENT WAS UNABLE TO BE CONFIRMED AS THE LOT NUMBER OF DEVICE INVOLVED IN THE INCIDENT IS UNKNOWN. DEVICE HISTORY RECORD REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. 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. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 1825034-2017-02284, 02735.

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE THAT THE PATIENT EXPERIENCED PAIN APPROXIMATELY 3 MONTHS POST-IMPLANTATION OF AN ELBOW PROSTHESIS. NO FURTHER INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
316630 EXPLOR 2X26MM IMPLANT STEM WITH SCREW PROSTHESIS, ELBOW KWI BIOMET ORTHOPEDICS N/A NI

Patients

Seq Age Sex Outcome Treatment
1 64 YR Other