FDA Adverse Event Summary report: N

DEPUY ACETABULAR

MDR report key: 2954155 · Received January 25, 2013

Report

Report Number
MW5028894
Date Received
January 25, 2013
Date of Event
October 10, 2011
Report Date
January 25, 2013
Manufacturer
DEPUY
Product Code
LPH
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
FL, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

I HAD A DEPUY HIP REPLACEMENT IN 2011. TWO WEEKS LATER, MY HIP DISLOCATED AND THEN DISLOCATED THREE TIMES MORE. I DON'T MOVE OFF THE SOFA EXCEPT TO GO TO BED. MY PAIN IS UNBEARABLE. I HAVE A LARGE LUMP ON MY SIDE. WORST THING IS I CANNOT FIND AN ORTHO SURGEON THAT WANT TO DO THE REVISION. I AM SUFFERING EVERY DAY. I NEED HELP. DEPUY MODEL NUMBERS 1217-35-500, 1221-40-458, 1217-32-058, 1012-04-050, 1365-40-730 ARE ALL THE PART NUMBERS. CAN SOMEONE FROM THE FDA HELP ME PLEASE. I HAVE PARTIAL DISLOCATIONS ALL THE TIME AND NEED HELP, WITH MANY GRAND KIDS I CANNOT PLAY WITH ANY MORE DUE TO THIS HIP. LIFE IN THIS PAIN IS SURE NOT WORTH ANY QUALITY OF LIFE TO EXIST FOR. MY FAMILY IS WORRIED AND DO NOT KNOW WHAT TO DO FOR ME. THEY TRY TO TAKE CARE OF ME BUT I AM USED TO CARING FOR THEM. I MISS MY LIFE BEFORE THIS HIP SURGERY. WHAT A MISTAKE, BUT WAS TOLD BEFORE SURGERY BY DOCTOR I WILL FEEL WONDERFUL AFTER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
35337 DEPUY ACETABULAR NONE LPH DEPUY 1217-32-058
35338 DEPUY LINER HIP LINER LPH DEPUY 1221-40-258
35396 DEPUY PINN W/ GRIPTION 58MM HIP SYSTEM LPH DEPUY 121735500, 122140458
35397 DEPUY FEMORAL STEM HIP FEMORAL STEM LPH DEPUY 1012-04-050
35398 DEPUY STEM HIP STEM LPH DEPUY 1365-40-730

Patients

Seq Age Sex Outcome Treatment
1 64 YR Hospitalization| O| R| S