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 |