BIOMET OFFSET LOCKING INSERT NEUTRAL
Received Dec 16, 2011 · Event occurred Nov 21, 2011
Report 0001825034-2011-01139 · MDR key 2379791
Device
Generic name
Prosthesis, Knee
Manufacturer
Biomet OrthopedicsModel number
N/ACatalog number
141494
Lot number
280700
Product problems
- Insufficient Device Problem Information
Patient
Not reported
- Unspecified Infection
Narrative
Additional Manufacturer Narrative
THE USER FACILITY IS OUTSIDE OF THE UNITED STATES. NO MEDWATCH REPORT WAS RECEIVED. 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 TWO STATES, "EARLY OR LATE POSTOPERATIVE INFECTION, AND ALLERGIC REACTION". REVIEW OF STERILIZATION CERTIFICATION CONFIRMS DEVICE WAS STERILIZED IN ACCORDANCE WITH ISO (B)(4). THIS REPORT IS NUMBER 2 OF 8 MDRS FILED FOR THE SAME EVENT (REFERENCE 1825034-2011-01138 THROUGH 01145).
Description of Event or Problem
IT WAS REPORTED THAT PATIENT UNDERWENT TOTAL KNEE ARTHROPLASTY ON (B)(6) 2010. SUBSEQUENTLY, THE PATIENT WAS REVISED ON (B)(6), DUE TO INFECTION. ALL PREVIOUS IMPLANTS EXCEPT FOR THE PATELLA BUTTON WERE REMOVED AND REPLACED.