FDA Adverse Event Injury Summary report: N

EPOLY 32MM RLC LNR MROM SZ23

MDR report key: 7759395 · Received August 7, 2018

Report

Report Number
0001825034-2018-05810
Event Type
Injury
Date Received
August 7, 2018
Date of Event
March 19, 2014
Report Date
October 17, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JDI
PMA / PMN Number
PK070364
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 0

UPON REASSESSMENT OF THE REPORTED EVENT, THIS REPORT SHOULD BE VOIDED AS IT WAS DETERMINED TO BE A DUPLICATE OF MFR NUMBER 0001825034-2014-04620.

Additional Manufacturer Narrative · 1

(B)(4). CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION, AS THE DEVICE LOCATION IS UNKNOWN. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. UNIQUE IDENTIFIER (UDI) #: N/A. CONCOMITANT MEDICAL PRODUCTS: ITEM # 51-107100, STEM, LOT # 2811558; ITEM # 650-1056, HEAD, LOT # 302990; ITEM # 11-104050, SHELL, LOT # 300900; ITEM # 650-1065, TAPER SLEVE, LOT # 190990. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2018-05807, 0001825034-2018-05808, 0001825034-2018-05809, 0001825034-2018-05811.

Description of Event or Problem · 1

IT WAS REPORTED THAT APPROXIMATELY 1 YEAR POST IMPLANTATION, THE PATIENT WAS NOTED TO HAVE CONTINUED COMPLAINTS OF PAIN AND WAS FOUND TO HAVE A MRSA INFECTION. THE PATIENT SUBSEQUENTLY UNDERWENT A TWO-STAGE REVISION, WITH ANTIBIOTIC SPACERS PLACED DURING THIS EVENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
598354 EPOLY 32MM RLC LNR MROM SZ23 PROSTHESIS, HIP JDI ZIMMER BIOMET, INC. N/A 590610

Patients

Seq Age Sex Outcome Treatment
1 49 YR Hospitalization| R