FDA Adverse Event Injury Summary report: N

UNKNOWN AGC FEMORAL

MDR report key: 6577910 · Received May 19, 2017

Report

Report Number
3002806535-2017-00379
Event Type
Injury
Date Received
May 19, 2017
Date of Event
April 7, 2010
Report Date
May 19, 2017
Manufacturer
BIOMET UK LTD.
Product Code
JWH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS - UNKNOWN AGC BEARING AND UNKNOWN AGC TIBIAL TRAY. FOREIGN REPORT SOURCE: (B)(4). REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVISE HISTORY RECORDS REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. COMPLAINT HISTORY COULD NOT BE CONDUCTED AS THE PRODUCT IDENTIFICATION IS UNKNOWN. 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. MULTIPLE MDRS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 3002806535-2017-003780 AND 3002806535-2017-00381.: PRODUCT LOCATION UNKNOWN.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT UNDERWENT A RIGHT KNEE ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT UNDERWENT A REVISION PROCEDURE DUE TO DISSOCIATION AND PERI-PROSTHETIC FRACTURE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
360220 UNKNOWN AGC FEMORAL PROSTHESIS, KNEE JWH BIOMET UK LTD.

Patients

Seq Age Sex Outcome Treatment
1 86 YR Hospitalization| R SEE NARRATIVE IN H10