FDA Adverse Event Injury Summary report: N

UNKNOWN OXFORD BEARING

MDR report key: 6789851 · Received August 11, 2017

Report

Report Number
3002806535-2017-00822
Event Type
Injury
Date Received
August 11, 2017
Date of Event
May 10, 2017
Report Date
August 11, 2017
Manufacturer
BIOMET UK LTD.
Product Code
JWH
PMA / PMN Number
PN/A
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4) INITIAL REPORTER: HUAMING XUE, YIHUI TU, TONG MA, TAO WEN, TAO YANG, MINWEI CAI ¿UP TO TWELVE YEAR FOLLOW-UP OF THE OXFORD PHASE THREE UNICOMPARTMENTAL KNEE REPLACEMENT IN CHINA: SEVEN HUNDRED AND EIGHT KNEES FROM AN INDEPENDENT CENTRE¿ INTERNATIONAL ORTHOPAEDICS (SICOT) DOI 10.1007/S00264-017-3492-4. THE REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. A DEVICE HISTORY RECORD REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. A COMPLAINT HISTORY REVIEW WAS UNABLE TO BE PERFORMED AS THE PART AND LOT NUMBERS ARE UNKNOWN. A ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. 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. PRODUCT LOCATION UNKNOWN.

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE THAT ONE PATIENT WAS REVISED TO ADDRESS A BEARING DISLOCATION. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
570549 UNKNOWN OXFORD BEARING PROSTHESIS, KNEE JWH BIOMET UK LTD. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R