FDA Adverse Event Injury Summary report: N

BI-METRIC/X POR NC LAT 16X160

MDR report key: 7151487 · Received December 28, 2017

Report

Report Number
0001825034-2017-11476
Event Type
Injury
Date Received
December 28, 2017
Date of Event
February 6, 2016
Report Date
December 27, 2017
Manufacturer
ZIMMER BIOMET, INC.
Product Code
LPH
PMA / PMN Number
PK030055
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: 11-173662 M2A 38 MM MOD HD STD NK LOT 806250, 15-105056 M2A 1 PC SHELL 38 MM X 56 MM LOT 590210. REPORTED EVENT WAS CONFIRMED BY REVIEW OF REVISION OP NOTES. REVIEW OF REVISION NOTES , FOUND THAT THE DIAGNOSIS INCLUDES INFECTED LEFT TOTAL HIP ARTHROPLASTY, ACUTE LEFT LOWER EXTREMITY DEEP VENOUS THROMBOSIS, SEPSIS WITH COAGULASE-NEGATIVE STAPHYLOCOCCUS, CORONARY ARTERY DISEASE, A MYOCARDIAL INFARCTION, GASTRITIS, ANEMIA, CHRONIC PAIN AND MORBID OBESITY IT IS NOTED THAT THERE IS A BLOOD LOSS. DHR WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. REVIEW OF THE COMPLAINT HISTORY DETERMINED THAT NO FURTHER ACTION IS REQUIRED AS NO WERE TRENDS IDENTIFIED. ROOT CAUSE COULD NOT BE DETERMINED WITH INFORMATION AVAILABLE. 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.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING A HIP PROCEDURE, PATIENT REQUIRED A BLOOD TRANSFUSION ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
931985 BI-METRIC/X POR NC LAT 16X160 HIP PROSTHESIS LPH ZIMMER BIOMET, INC. N/A 370020

Patients

Seq Age Sex Outcome Treatment
1 58 YR Hospitalization| R