FDA Adverse Event Injury Summary report: N

UNKNOWN HIP

MDR report key: 6299052 · Received February 2, 2017

Report

Report Number
0001822565-2017-00443
Event Type
Injury
Date Received
February 2, 2017
Report Date
January 30, 2017
Manufacturer
ZIMMER, INC.
Product Code
JDI
PMA / PMN Number
PNI
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A CONCLUSION AS TO THE CAUSE OF THE EVENT. THE PRODUCT IDENTIFICATION NECESSARY TO REVIEW MANUFACTURING HISTORY WAS NOT PROVIDED. MATTHIEU OLLIVIER, ET AL. ¿USE OF POROUS TANTALUM COMPONENTS IN PAPROSKY TWO AND THREE ACETABULAR REVISION. A MINIMUM FIVE-YEAR FOLLOW-UP OF FIFTY ONE HIPS.¿ 10.1007/S00264-016-3312-2.

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE THAT A PATIENT EXPERIENCED A FRACTURED SCREW IN ONE HIP AND A HARRIS HIP SCORE OF 78. NO REVISION PROCEDURE WAS REPORTED AND PATIENT OUTCOME IS UNKNOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
78815 UNKNOWN HIP PROSTHESIS, HIP JDI ZIMMER, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Other