FDA Adverse Event Injury Summary report: N

UNKNOWN TIBIAL COMPONENT

MDR report key: 7192806 · Received January 16, 2018

Report

Report Number
3002806535-2018-00088
Event Type
Injury
Date Received
January 16, 2018
Report Date
January 16, 2018
Manufacturer
BIOMET UK LTD.
Product Code
HRY
PMA / PMN Number
PNI
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4) PANZRAM B, BERTLICH I, REINER T, WALKER T, HAGMANN S, GOTTERBARM T (2017) CEMENTLESS OXFORD MEDIAL UNICOMPARTMENTAL KNEE REPLACEMENT: AN INDEPENDENT SERIES WITH A 5-YEAR-FOLLOW-UP. ARCHIVES OF ORTHOPAEDIC AND TRAUMA SURGERY, JULY 2017, VOLUME 137, ISSUE 7, PP 1011¿1017, HTTPS://LINK.SPRINGER.COM/CONTENT/PDF/10.1007/S00402-017-2696-9.PDF (B)(6). REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DHR REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. ROOT CAUSE WAS UNABLE TO BE DETERMINED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

Description of Event or Problem · 1

INFORMATION RECEIVED BASED ON REVIEW OF A JOURNAL ARTICLE, ENTITLED "CEMENTLESS OXFORD MEDIAL UNICOMPARTMENTAL KNEE REPLACEMENT: AN INDEPENDENT SERIES WITH A 5-YEAR-FOLLOW-UP", BY PANZRAM, B. ET AL. (2017) THIS COMPLAINT REFERS TO THE REPORTED REVISION DUE TO POST TRAUMATIC TIBIAL PLATEAU FRACTURE. IT WAS REVISED TO ORIF AND TKR WITH UNKNOWN CEMENTED FEMORAL, TIBIAL AND BEARING COMPONENTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
36580 UNKNOWN TIBIAL COMPONENT HRY BIOMET UK LTD. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R