BIOMET TAPERLOC FEMORAL STEM
Report
- Report Number
- 0001825034-2018-01650
- Event Type
- Injury
- Date Received
- March 5, 2018
- Report Date
- March 2, 2018
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- JDI
- PMA / PMN Number
- PK050441
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MS, US
- Reporter Occupation
- PATIENT
Narratives
CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION, AS DEVICES REMAIN IMPLANTED. CONCOMITANT MEDICAL PRODUCTS: ITEM# 16-104150, RINGLOC SHELL, LOT# 847500. ITEM# EP-108323, E-POLY LINER, LOT# 301360. ITEM# 11-363662, FEMORAL HEAD, LOT# 047130. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DHR WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. REVIEW OF THE COMPLAINT HISTORY DETERMINED THAT NO FURTHER ACTION IS REQUIRED. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS. MULTIPLE REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2018-00376-1, 0001825034-2018-00377-1, 0001825034-2018-01649.
IT WAS REPORTED THAT A PATIENT STARTED EXPERIENCING PAIN 4 YEARS POST IMPLANTATION. THE PATIENT IS EXPERIENCING WORSENING PAIN, A LIMP, AMBULATION DIFFICULTIES, MUSCLE SPASMS, MUSCLE DAMAGE, AND NUMBNESS FROM HIP DOWN TO TOES FOR THE PAST 2 YEARS. PATIENT ALSO ALLEGES THAT THE HIP "TRIED TO DISLOCATE" ON TWO OCCASIONS. PATIENT REPORTS BEING PRESCRIBED PERCOCET FOR PAIN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 158422 | BIOMET TAPERLOC FEMORAL STEM | HIP PROSTHESIS | JDI | ZIMMER BIOMET, INC. | N/A | 606010 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |