inforMED
InjuryMBV

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 Orthopedics

Model number

N/A

Catalog 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.