BIOMET ILOK PRI TIB TRAY 71MM
Received Nov 18, 2015 · Event occurred Sep 22, 2014
Report 0001825034-2015-04718 · MDR key 5233748
Device
Generic name
Prosthesis, Knee
Manufacturer
Biomet OrthopedicsModel number
N/ACatalog number
141213
Lot number
180980
Product problems
- Patient-Device Incompatibility
Patient
64 YR
- Hypersensitivity/Allergic reaction
Narrative
Additional Manufacturer Narrative
THIS FOLLOW-UP REPORT IS BEING FILED TO RELAY ADDITIONAL INFORMATION, WHICH WAS UNKNOWN AT THE TIME OF THE INITIAL MEDWATCH. (B)(4). 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 4 STATES, "LOOSENING OR MIGRATION OF THE IMPLANTS CAN OCCUR DUE TO LOSS OF FIXATION, TRAUMA, MALALIGNMENT, BONE RESORPTION, AND EXCESSIVE ACTIVITY." NUMBER 6 STATES, "INADEQUATE RANGE OF MOTION DUE TO IMPROPER SELECTION OR POSITIONING OF COMPONENTS." NUMBER 15 STATES, "INTEROPERATIVE OR POSTOPERATIVE BONE FRACTURE AND/OR POSTOPERATIVE PAIN." THIS REPORT IS BASED ON ALLEGATIONS SET FORTH IN PLAINTIFF¿S COMPLAINT AND THE ALLEGATIONS CONTAINED THEREIN ARE UNVERIFIED. THIS REPORT IS NUMBER 2 OF 4 MDRS FILED FOR THE SAME EVENT (REFERENCE 1825034-2015-04718 / 04719 / 04720 / 04721). PRODUCT LOCATION UNKNOWN.
Description of Event or Problem
LEGAL COUNSEL FOR PATIENT REPORTED THAT PATIENT UNDERWENT TOTAL RIGHT KNEE ARTHROPLASTY ON (B)(6) 2013. SUBSEQUENTLY, PATIENT'S LEGAL COUNSEL FURTHER REPORTS PATIENT ALLEGATIONS OF POSSIBLE NICKEL ALLERGY. THERE HAS BEEN NO REPORTED REVISION PROCEDURE. THIS REPORT IS BASED ON ALLEGATIONS SET FORTH IN PLAINTIFF'S COMPLAINT AND THE ALLEGATIONS CONTAINED THEREIN ARE UNVERIFIED. ADDITIONAL INFORMATION RECEIVED FROM PATIENT'S LEGAL COUNSEL NOTED A REVISION PROCEDURE WAS PERFORMED ON (B)(6) 2014 DUE TO PATIENT ALLEGATIONS OF LOOSENING OF THE FEMORAL COMPONENT WITH VARUS COLLAPSE, NICKEL, ALUMINUM AND IRON ALLERGY, METAL DEBRIS, BONE EROSION WITH INFLAMMATORY SYNOVITIS, PAIN, SWELLING, EFFUSION, DIFFICULTY AMBULATING AND CREPITUS.
Additional Manufacturer Narrative
THIS FOLLOW-UP REPORT IS BEING FILED TO RELAY ADDITIONAL INFORMATION, WHICH WAS UNKNOWN AT THE TIME OF THE INITIAL MEDWATCH. (B)(4).
Description of Event or Problem
LEGAL COUNSEL FOR PATIENT REPORTED THAT PATIENT UNDERWENT TOTAL RIGHT KNEE ARTHROPLASTY ON (B)(6) 2013. SUBSEQUENTLY, PATIENT'S LEGAL COUNSEL FURTHER REPORTS PATIENT ALLEGATIONS OF POSSIBLE NICKEL ALLERGY. ADDITIONAL INFORMATION RECEIVED FROM PATIENT'S LEGAL COUNSEL NOTED A REVISION PROCEDURE WAS PERFORMED ON (B)(6) 2014 DUE TO PATIENT ALLEGATIONS OF LOOSENING OF THE FEMORAL COMPONENT WITH VARUS COLLAPSE, NICKEL, ALUMINUM AND IRON ALLERGY, METAL DEBRIS, BONE EROSION WITH INFLAMMATORY SYNOVITIS, PAIN, SWELLING, EFFUSION, DIFFICULTY AMBULATING AND CREPITUS. THIS REPORT IS BASED ON ALLEGATIONS SET FORTH IN PLAINTIFF'S COMPLAINT AND THE ALLEGATIONS CONTAINED THEREIN ARE UNVERIFIED. ADDITIONAL INFORMATION RECEIVED IN OPERATIVE NOTES REPORTED THAT PATIENT UNDERWENT A REVISION PROCEDURE ON (B)(6) 2014 DUE TO ASEPTIC LOOSENING OF THE FEMORAL COMPONENT WITH NICKEL ALLERGY. DURING THE PROCEDURE, METAL DEBRIS, THE REMOVAL OF INFLAMMATORY SYNOVIAL TISSUE, LOOSENING OF THE FEMORAL COMPONENT WITH VARUS COLLAPSE AND FEMORAL CONDYLAR BONE EROSION WERE NOTED. THE FEMORAL COMPONENTS, TIBIAL COMPONENTS AND TIBIAL BEARING WERE REMOVED AND REPLACED WITH COMPETITOR PRODUCT.
Additional Manufacturer Narrative
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 2 STATES, ¿EARLY OR LATE POSTOPERATIVE INFECTION AND ALLERGIC REACTION.¿ THIS REPORT IS BASED ON ALLEGATIONS SET FORTH IN PLAINTIFF¿S COMPLAINT AND THE ALLEGATIONS CONTAINED THEREIN ARE UNVERIFIED. THIS REPORT IS NUMBER 1 OF 4 MDRS FILED FOR THE SAME EVENT (REFERENCE 1825034-2015-04718 / 04719 / 04720 / 04721).
Description of Event or Problem
LEGAL COUNSEL FOR PATIENT REPORTED THAT PATIENT UNDERWENT TOTAL RIGHT KNEE ARTHROPLASTY ON (B)(6), 2013. SUBSEQUENTLY, PATIENT'S LEGAL COUNSEL FURTHER REPORTS PATIENT ALLEGATIONS OF POSSIBLE NICKEL ALLERGY. THERE HAS BEEN NO REPORTED REVISION PROCEDURE. THIS REPORT IS BASED ON ALLEGATIONS SET FORTH IN PLAINTIFF'S COMPLAINT AND THE ALLEGATIONS CONTAINED THEREIN ARE UNVERIFIED.