MLRY-HD LAT POR FEMORAL 11MM
Report
- Report Number
- 0001825034-2013-05284
- Event Type
- Injury
- Date Received
- November 13, 2013
- Report Date
- October 14, 2013
- Manufacturer
- BIOMET ORTHOPEDICS
- Product Code
- LPH
- PMA / PMN Number
- PK030055
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- PHYSICIAN
Narratives
CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. REVIEW OF DEVICE HISTORY RECORDS SHOW THAT LOT RELEASED WITH NO RECORDED ANOMALY OR DEVIATION. THERE ARE WARNINGS IN THE PACKAGE INSERT THAT STATE THAT THIS TYPE OF EVENT CAN OCCUR: UNDER POSSIBLE ADVERSE EFFECTS, NUMBER 1 STATES, ¿MATERIAL SENSITIVITY REACTIONS.¿ NUMBER 15 STATES, ¿ELEVATED METAL ION LEVELS HAVE BEEN REPORTED WITH METAL-ON-METAL ARTICULATING SURFACES.¿ THIS REPORT IS NUMBER 3 OF 8 MDRS FILED FOR THE SAME PATIENT (REFERENCE 1825034-2013-02313-1/02314-1 AND 05284/05289).
BIOMET ORTHOPEDICS RECEIVED PRELIMINARY CLINICAL DATA FROM DR (B)(6) REGARDING PATIENTS ENROLLED IN A (B)(4). IT WAS REPORTED THAT PATIENT UNDERWENT A RIGHT TOTAL HIP ARTHROPLASTY ON (B)(6) 2007 AND A LEFT TOTAL HIP ARTHROPLASTY (B)(6) 2008. DURING POST OPERATIVE MONITORING AND TESTING A SOLID MASSES WERE NOTED. THE MASS ON THE LATERAL AREA OF THE RIGHT HIP MEASURED 3 X 2.9 X 5.4 CM AND THE MASS ON THE ANTERIOR AREA OF THE LEFT HIP MEASURED 2.7 X 3.5 X 1.4 CM. THESE FINDINGS WERE FOUND DUE TO FOLLOW UP TESTING. NO FURTHER INFORMATION HAS BEEN PROVIDED AT THIS TIME.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 586955 | MLRY-HD LAT POR FEMORAL 11MM | PROSTHESIS, HIP | LPH | BIOMET ORTHOPEDICS | N/A | 589450 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R |