FDA Adverse Event Injury Summary report: N

OSS POLY TIBIAL BUSHING

MDR report key: 7433661 · Received April 16, 2018

Report

Report Number
0001825034-2018-02799
Event Type
Injury
Date Received
April 16, 2018
Report Date
May 15, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JDI
PMA / PMN Number
PK002757
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: 163662, 28MM MOD HD STD NECK TP1 TAPER, 494560, 11-165218, RINGLOC BI-POLAR 28X47MM, 382420, 150478, OSS POLY LOCK PIN, 610340, 161034, OSS RS POLY FEM BUSHINGS SET/2, 252670, 150410, OSS TIBIAL POLY BEARING 12MM, 837020. CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 - 2018 - 02798, 0001825034 - 2018 - 02799, 0001825034 - 2018 - 02797, 0001825034 - 2018 - 02801, 0001825034 - 2018 - 02802. REMAINS IMPLANTED.

Additional Manufacturer Narrative · 1

UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED THAT THIS DEVICE WAS NOT INVOLVED IN THE EVENT. THE INITIAL REPORT WAS SUBMITTED IN ERROR AND SHOULD BE VOIDED.

Description of Event or Problem · 1

IT WAS REPORTED PATIENT IS EXPERIENCING NICKEL ALLERGY THREE YEARS POST-IMPLANTATION. NO REVISION HAS BEEN REPORTED TO DATE. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE IS AVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
276124 OSS POLY TIBIAL BUSHING PROSTHESIS, HIP JDI ZIMMER BIOMET, INC. N/A 594960

Patients

Seq Age Sex Outcome Treatment
1 Other