FDA Adverse Event Injury Summary report: N

HIP REPLACEMENT SYSTEM

MDR report key: 7237807 · Received February 1, 2018

Report

Report Number
MW5075024
Event Type
Injury
Date Received
February 1, 2018
Date of Event
May 8, 2012
Report Date
January 31, 2018
Manufacturer
DEPUY
Product Code
JDI
Report Source
Voluntary report
Reporter Location
FL, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

I HAD A LEFT HIP REPLACEMENT WITH A DEPUY PRODUCT. THREE MODEL NUMBERS ARE LISTED. MODEL 1217-22-054, 1217-20-500 AND 1570-11-135. ALSO, 1221-36-054 AND 1365-52-000. AFTER SURGERY I EXPERIENCED A FRACTURE WHICH TOOK ME A YEAR TO RECOVER FROM. MY LEFT LEG IS AN INCH SHORTER NOW. I AM WRITING YOU TO LET YOU KNOW THAT MY LEFT HIP DOES, ON OCCASION, UNLOCK AND LOCK MY CAR AS I AM APPROACHING IT ON THE LEFT SIDE. HAS HAPPENED 15 TIMES OVER PAST 6 YEARS. I HAVE HAD WITNESSES. CAN YOU PLEASE INVESTIGATE AND REPLY. THANK YOU.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
77875 HIP REPLACEMENT SYSTEM HIP REPLACEMENT SYSTEM JDI DEPUY 1365-52-000

Patients

Seq Age Sex Outcome Treatment
1 73 YR Disability