FDA Adverse Event Death Summary report: N

UNKNOWN NEXGEN FEMORAL COMPONENT

MDR report key: 6642959 · Received June 15, 2017

Report

Report Number
0001822565-2017-04102
Event Type
Death
Date Received
June 15, 2017
Date of Event
July 25, 2013
Report Date
June 15, 2017
Manufacturer
ZIMMER, INC.
Product Code
JWH
PMA / PMN Number
PNI
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). INITIAL REPORTER - THE ARTICLE WAS WRITTEN BY MARIANO FERNANDEZ-FAIREN, DANIEL HERNANDEZ-VAQUERO, ANTONIO MURCIA, ANA TORRES, RAFAEL LLOPIS THE COMPLAINT DEVICE IS NOT EXPECTED FOR RETURN CURRENTLY, BUT A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED UPON RECEIPT OF ADDITIONAL INFORMATION. FERNANDEZ-FAIREN, ET AL. " TRABECULAR METAL IN TOTAL KNEE ARTHROPLASTY ASSOCIATED WITH HIGHER KNEE SCORES: A RANDOMIZED" CLIN ORTHOP RELAT RES (2013) 471:3543¿3553. 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: 0001822565-2017- 04099, 0001822565-2017-04101 AND 0001822565-2017-04102.

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE THAT 1 PATIENT DIED DUE TO UNKNOWN REASONS WITH IMPLANTS IN SITU AFTER A KNEE ARTHROPLASTY ON AN UNKNOWN DATE. NO FURTHER INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
425732 UNKNOWN NEXGEN FEMORAL COMPONENT PROSTHESIS, KNEE JWH ZIMMER, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Death