FDA Adverse Event Injury Summary report: N

UNKNOWN OXFORD TIBIAL COMPONENT

MDR report key: 7272828 · Received February 15, 2018

Report

Report Number
3002806535-2018-00305
Event Type
Injury
Date Received
February 15, 2018
Report Date
February 15, 2018
Manufacturer
BIOMET UK LTD.
Product Code
HRY
PMA / PMN Number
PN/A
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
DA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4) PER W. KRISTENSEN, MD, HENRIETTE A. HOLM, RN, CLAUS VARNUM, MD. UP TO 10-YEAR FOLLOW-UP OF THE OXFORD MEDIAL PARTIAL KNEE ARTHROPLASTY ¿ 695 CASES FROM A SINGLE INSTITUTION. THE JOURNAL OF ARTHROPLASTY 28 SUPPL. 2 (2013) 195¿198. (B)(6). REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER AS THE LOT NUMBERS OF THE DEVICES ARE UNKNOWN, DHR REVIEWS COULD NOT BE PERFORMED. ROOT CAUSE COULD NOT BE DETERMINED. IF FURTHER INFORMATION IS FOUND THAT WOULD CHANGE OR ALTER ANY CONCLUSIONS REACHED, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY.

Description of Event or Problem · 1

INFORMATION RECEIVED BASED ON JOURNAL ARTICLE ENTITLED "UP TO 10-YEAR FOLLOW-UP OF THE OXFORD MEDIAL PARTIAL KNEE ARTHROPLASTY ¿ 695 CASES FROM A SINGLE INSTITUTION", BY W. KRISTENSEN, ET AL. (2013) ABSTRACT PARTIAL KNEE ARTHROPLASTY (PKA) HAS SHOWN OBVIOUS ADVANTAGES COMPARED TO TOTAL KNEE ARTHROPLASTY, BUT SURVIVAL OF PKA FROM DIFFERENT INSTITUTIONS AND REGISTRIES HAS DIFFERED. IN OUR INSTITUTION, 695 CONSECUTIVE OXFORD MEDIAL PKAS WERE PERFORMED FROM 2002 TO 2011 WITH MEAN FOLLOW-UP OF 4.6 YEARS. (B)(4). THIS COMPLAINTS REFERS TO FOUR KNEE REVISIONS DUE TO DEEP INFECTION (PAGE 197, TABLE 2)

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
118371 UNKNOWN OXFORD TIBIAL COMPONENT PROSTHESIS, KNEE HRY BIOMET UK LTD. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R