M2A TPR HI CARBON 41/32MM LNR
Report
- Report Number
- 0001825034-2013-04231
- Event Type
- Injury
- Date Received
- September 27, 2013
- Date of Event
- August 27, 2013
- Report Date
- August 29, 2013
- Manufacturer
- BIOMET ORTHOPEDICS
- Product Code
- KWY
- PMA / PMN Number
- PK003363
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- 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." THIS REPORT IS NUMBER 3 OF 3 MDRS FILED FOR THE SAME EVENT (REFERENCE 1825034-2013-04229 / 04231).
EXAMINATION OF RETURNED DEVICE FOUND NO EVIDENCE OF PRODUCT NON-CONFORMANCES. MODERATE WEAR WAS NOTED ON THE MODULAR HEAD THIS REPORT IS NUMBER 3 OF 3 MDRS FILED FOR THE SAME EVENT (REFERENCE 1825034-2013-04229-1/04231-1).
IT WAS REPORTED PATIENT UNDERWENT A TOTAL HIP ARTHROPLASTY ON (B)(6) 2010. SUBSEQUENTLY, PATIENT WAS REVISED ON (B)(6) 2013, DUE TO SWELLING AND PSEUDOTUMOR. NO FURTHER INFORMATION HAS BEEN PROVIDED TO DATE.
IT WAS REPORTED PATIENT UNDERWENT A RIGHT TOTAL HIP ARTHROPLASTY ON (B)(6), 2010. SUBSEQUENTLY, PATIENT WAS REVISED ON (B)(6), 2013 DUE TO SWELLING AND PSEUDOTUMOR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 489988 | M2A TPR HI CARBON 41/32MM LNR | PROSTHESIS, HIP | KWY | BIOMET ORTHOPEDICS | N/A | 019610 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 66 YR | Hospitalization| R |