FDA Adverse Event Injury Summary report: N

FEMORAL HEAD

MDR report key: 7201773 · Received January 17, 2018

Report

Report Number
0002648920-2018-00047
Event Type
Injury
Date Received
January 17, 2018
Report Date
March 23, 2018
Manufacturer
ZIMMER MANUFACTURING B.V.
Product Code
LPH
PMA / PMN Number
PK953337
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

(B)(4) MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT. PLEASE SEE REPORTS: 0001822565-2018-00392, 0001822565-2018-00393, 0001822565-2018-00394, 0001822565-2018-00395. CONCOMITANT MEDICAL PRODUCTS: 00784800200 MODULAR NECK K 12/14 NECK TAPER USE WITH +0 HEADS ONLY LOT 61218348, 00771301300 MODULAR FEMORAL STEM PRESS-FIT PLASMA SPRAYED CEMENTLESS SIZE 13.5 LOT 61375744, 65620005422 SHELL POROUS WITH CLUSTER HOLES 54 MM O.D. WITH CALCICOAT CERAMIC COATING LOT 61330651, 00631005032 LINER 10 DEGREE ELEVATED RIM 32 MM I.D. FOR USE WITH 50/52/54 MM O.D. SHELLS LOT 61365043. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. DEVICE REMAINS IMPLANTED.

Additional Manufacturer Narrative · 1

UPON REASSESSMENT OF THE REPORTED EVENT IT WAS DETERMINED THAT THIS EVENT WILL BE REPORTED ON MFR NUMBER 1822565-2011-02059-1.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT UNDERWENT A LEFT INITIAL TOTAL HIP ARTHROPLASTY DUE TO DEGENERATIVE ARTHRITIS. SUBSEQUENTLY, THE PATIENT IS EXPERIENCING SEVERE PAIN IN THE GROIN AND TIBIAL AREA. THE PATIENT HAS BEEN DOING ONGOING TREATMENT FOR THIS PAIN WITH MULTIPLE PROCEDURES AND IS REFUSING A REVISION PROCEDURE. NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
46282 FEMORAL HEAD PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED LPH ZIMMER MANUFACTURING B.V. N/A 61426909

Patients

Seq Age Sex Outcome Treatment
1 Other