FDA Adverse Event Injury Summary report: N

KNEE PROSTHESIS

MDR report key: 21903507 · Received April 24, 2025

Report

Report Number
MW5169507
Event Type
Injury
Date Received
April 24, 2025
Report Date
April 24, 2025
Manufacturer
DEPUY SYNTHES
Product Code
JWH
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
OTHER
Health Professional
*

Narratives

Description of Event or Problem · 0

PATIENT: (B)(6), RECEIVED TWO KNEE REPLACEMENT, FIRST ON (B)(6) 2016 AND THE SECOND (B)(6) 2019. I AM A RETIRED MILITARY ENLISTED(SFC) ARMY, AND I NEED SOME HELP IN THIS MATTER, I WENT BACK TO MY DOCTOR/SURGEON TO TALK TO HIM ABOUT THE PROBLEM I WAS HAVING. HE TOLD ME THAT HE DID EVERYTHING RIGHT, AND THE ONLY THING HE COULD DO WAS TO ¿GO BACKING¿¿. I LEFT HIS OFFICE AND FOUND INFORMATION ONLINE ABOUT DUPEY SYNTHES HAVING KNEE REPLACEMENT PART RECALLS. THEN, I MADE AN APPOINTMENT TO SEE THE SURGEON AGAIN, WENT BACK TO HIS OFFICE. HE EXAMINED BOTH KNEES AND TOOK X-RAYS AND STATED THAT EVERYTHING LOOKS GREAT TO HIM. AFTER HE GAVE ME HIS DIAGNOSIS, I SHOWED HIM THE INFORMATION THAT I FOUND ON THE INTERNET, AND HE STATED TO ME AND MY WIFE, THAT IT WAS AMBULANCE CHASERS. HE TOLD US BOTH THAT IT IS SOMETHING THAT HAPPENS ALL THE TIME ON THE NET, JUST IGNORE IT. I AM EXPERIENCING SIGNIFICANT PAIN AND NEED ASSISTANCE SOON. I HAVE A KNEE REPLACEMENT PATIENT L.D. CARD FROM DEPUY SYNTHES- 25M0316/DSUS/JRC/0216/1386 PROVIDED BY (B)(6) M.D., ON (B)(6) 2019. IF THERE IS ANYTHING YOUR OFFICE CAN DO FOR ME IN THIS MATTER. IT WOULD-BE VERY MUCH APPRECIATED. "THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2)". REF REPORT: MW5169506.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1226334 KNEE PROSTHESIS PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL JWH DEPUY SYNTHES

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown