FDA Adverse Event Injury Summary report: N

VANGUARD PS FEMORAL COMPONENT

MDR report key: 8028903 · Received November 1, 2018

Report

Report Number
0001825034-2018-10128
Event Type
Injury
Date Received
November 1, 2018
Report Date
October 31, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JWH
PMA / PMN Number
NI
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: BIOMET CC I-BEAM TRAY CAT#:141222, LOT#:UNK, VANGUARD PS TIBIAL BEARING CAT#: 183622, LOT#: UNK , UNKNOWN KNEE PATELLA CAT#:UNK, LOT#:UNK. CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION, AS THE PRODUCT LOCATION IS UNKNOWN .  REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD (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 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 MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 - 2018 - 10125 , 0001825034 - 2018 - 10126, 0001825034 - 2018 - 10127, 0001825034 - 2018 - 10128. PRODUCT LOCATION UNKNOWN.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT UNDERWENT TWO STAGE REVISION AFTER PRIMARY LEFT TOTAL KNEE ARTHROPLASTY DUE TO INFECTION. NO ADDITIONAL PATIENT CONSEQUENCES WERE REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
867699 VANGUARD PS FEMORAL COMPONENT PROSTHESIS, KNEE JWH ZIMMER BIOMET, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R