FDA Adverse Event Injury Summary report: N

UNKNOWN MILLER-GALANTE ARTICULAR SURFACE

MDR report key: 4941913 · Received July 23, 2015

Report

Report Number
1822565-2015-01286
Event Type
Injury
Date Received
July 23, 2015
Report Date
June 25, 2015
Manufacturer
ZIMMER, INC.
Product Code
JWH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FI
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

INFORMATION WAS RECEIVED VIA PUBLISHED LITERATURE. PLEASE REFERENCE LITERATURE AT THE FOLLOWING LOCATION: HTTP://LINK.SPRINGER.COM/ARTICLE/10.1007/S00402-008-0670-2. IT WAS REPORTED IN A JOURNAL ARTICLE THAT THREE KNEES WERE REVISED TO A TOTAL KNEE ARTHROPLASTY DUE TO WORN ARTICULAR SURFACE, WITHOUT PROGRESSION OF OA ON THE LATERAL SIDE OF ANY EVIDENCE OF LOOSENING OF THE COMPONENTS. THE ARTICLE INDICATES THAT ALL PATIENTS WERE IMPLANTED WITH A MILLER-GALANTE II UNICONDYLAR PROSTHESIS. THE PART AND LOT NUMBERS ARE UNKNOWN; THEREFORE THE DEVICE HISTORY RECORDS COULD NOT BE REVIEWED. THESE DEVICES ARE USED FOR TREATMENT OF PATIENTS. NO DEVICES OR PHOTOS WERE RECEIVED; THEREFORE THE CONDITION OF THE COMPONENTS IS UNKNOWN. OPERATIVE NOTES FOR PRIMARY AND REVISION SURGERIES WERE NOT PROVIDED. IT IS UNKNOWN WHETHER THE COMPONENTS WERE IMPLANTED WITH THE CORRECT FIT AND ORIENTATION AS PER THE SURGICAL TECHNIQUE. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED WITH THE INFORMATION PROVIDED.

Description of Event or Problem · 1

IT IS REPORTED THAT THREE KNEES WERE REVISED TO A TOTAL KNEE DUE TO A WORN UNICOMPARTMENTAL ARTICULAR SURFACE, WITHOUT PROGRESSION OF OSTEOARTHRITIS ON THE LATERAL SIDE OR ANY EVIDENCE OF LOOSENING OF THE COMPONENTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
480578 UNKNOWN MILLER-GALANTE ARTICULAR SURFACE KNEE PROSTHESIS JWH ZIMMER, INC.

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention