FDA Adverse Event Injury Summary report: N

EXPLOR 7X26MM IMPLANT STEM WITH SCREW

MDR report key: 6515819 · Received April 24, 2017

Report

Report Number
0001825034-2017-02546
Event Type
Injury
Date Received
April 24, 2017
Report Date
April 24, 2017
Manufacturer
BIOMET ORTHOPEDICS
Product Code
KWI
PMA / PMN Number
PK051385
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(6). INITIAL REPORTER - THE ARTICLE WAS WRITTEN BY SCHUYLER J HALVERSON, MIHIR J DESAI AND DONALD H LEE. THE COMPLAINT DEVICE IS NOT EXPECTED FOR RETURN CURRENTLY, BUT A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED UPON RECEIPT OF ADDITIONAL INFORMATION. HALVERSON ET AL. "CLINICAL OUTCOMES OF BIOMET EXPLOR MODULAR RADIAL HEAD ARTHROPLASTY SYSTEM" 37:853-858. PG. 1-33. THE REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. A DEVICE HISTORY RECORD REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. A COMPLAINT HISTORY REVIEW WAS UNABLE TO BE PERFORMED AS THE PART AND LOT NUMBERS ARE UNKNOWN. A ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS:0001825034-2017-02373.

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE THAT THE PATIENT EXPERIENCED MILD ELBOW AND WRIST PAIN APPROXIMATELY 38 MONTHS POST-IMPLANTATION OF A RIGHT RADIAL HEAD ARTHROPLASTY. NO FURTHER INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
298028 EXPLOR 7X26MM IMPLANT STEM WITH SCREW PROSTHESIS, SHOULDER KWI BIOMET ORTHOPEDICS N/A NI

Patients

Seq Age Sex Outcome Treatment
1 35 YR Other