FDA Adverse Event Injury Summary report: N

VANGUARD TIBIAL BEARING

MDR report key: 7763507 · Received August 8, 2018

Report

Report Number
0001825034-2018-06880
Event Type
Injury
Date Received
August 8, 2018
Date of Event
November 27, 2006
Report Date
September 4, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JWH
PMA / PMN Number
PK113550
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. 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.

Additional Manufacturer Narrative · 1

(B)(4). MEDICAL PRODUCTS: VANGUARD FEMORAL CATALOG # 183014 LOT # UNKNOWN, BIOMET CC I-BEAM TRAY 71MM CATALOG # 141225 LOT # UNKNOWN. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE WAS NOT RETURNED. 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 FILLED FOR THIS EVENT: 0001825034-2018-06878.

Description of Event or Problem · 1

IT WAS REPORTED A PATIENT UNDERWENT RIGHT PRIMARY TOTAL KNEE ARTHROPLASTY AND LATER THE PATIENT UNDERWENT MANIPULATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
604301 VANGUARD TIBIAL BEARING PROSTHESIS KNEE JWH ZIMMER BIOMET, INC. N/A UNK

Patients

Seq Age Sex Outcome Treatment
1 59 YR Hospitalization| R UNK PART/LOT, PATELLA