FDA Adverse Event Injury Summary report: N

UNKNOWN KUDO ELBOW

MDR report key: 6572569 · Received May 17, 2017

Report

Report Number
3002806535-2017-00384
Event Type
Injury
Date Received
May 17, 2017
Date of Event
August 12, 2013
Report Date
September 19, 2017
Manufacturer
BIOMET UK LTD.
Product Code
JDC
PMA / PMN Number
PK013042
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(6). THIS DEVICE IS NOT MANUFACTURED BY ZIMMER BIOMET IN THE UNITED STATES; HOWEVER, WE ARE FILING THIS REPORT AS ZIMMER BIOMET MANUFACTURES A SIMILAR DEVICE IN THE UNITED STATES UNDER 510K NUMBER K013042. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER AND NO PRODUCT WAS RETURNED. DHR AND COMPLAINT HISTORY COULD NOT BE REVIEWED DUE TO THE LACK OF INFORMATION RECEIVED. ROOT CAUSE WAS UNABLE TO BE DETERMINED. 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: 3002806535-2017-00384 AND 0001825034-2017-03281.

Additional Manufacturer Narrative · 1

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. IMPLANT DATE - UNKNOWN DATE IN 2007.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE CLINICAL PATIENT UNDERWENT AN ELBOW REVISION DUE TO ASEPTIC LOOSENING AND HUMERAL COMPONENT INSTABILITY APPROXIMATELY ONE YEAR POST-IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
355117 UNKNOWN KUDO ELBOW PROSTHESIS, ELBOW JDC BIOMET UK LTD. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 57 YR Hospitalization| R