FDA Adverse Event Injury Summary report: N

BIOMET CC I-BEAM TRAY 71MM

MDR report key: 7766716 · Received August 9, 2018

Report

Report Number
0001825034-2018-07497
Event Type
Injury
Date Received
August 9, 2018
Date of Event
September 13, 2007
Report Date
August 9, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
HRY
PMA / PMN Number
PK171054
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: VANGUARD CR ILOK FEM, CAT: 183028 ,LOT: UNK; VNGD CR TIB BRG, CAT: 183444 ,LOT: UNK; BIOMET ARCOM 3 PEG/POST ,CAT: UNK, LOT: UNK. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2018-07491, 0001825034-2018-07496, 0001825034-2018-07497, 0001825034-2018-07498. 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. PRODUCT NOT RETURNED.

Description of Event or Problem · 1

IT WAS REPORTED A PATIENT UNDERWENT A PRIMARY TOTAL KNEE ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT WAS NOTED TO HAVE PASSED THREE BLOODY STOOLS, AND WAS BLUE FROM TOES UP TO LEFT KNEE REQUIRING ADMISSION TO HOSPITAL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
609267 BIOMET CC I-BEAM TRAY 71MM KNEE, PROSTHESIS HRY ZIMMER BIOMET, INC. UNK

Patients

Seq Age Sex Outcome Treatment
1 80 YR Hospitalization| R