FDA Adverse Event Injury Summary report: N

ANCA FIT LINER

MDR report key: 9664361 · Received February 4, 2020

Report

Report Number
3010536692-2019-01084
Event Type
Injury
Date Received
February 4, 2020
Report Date
October 9, 2019
Manufacturer
HRY
Product Code
LPH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

THE DEVICE INVOLVED IS NOT REPORTABLE. PLEASE VOID THIS REPORT.

Description of Event or Problem · 1

ALLEGEDLY ATTENDED REVISION OF AN ANCA FIT HIP IMPLANTED 10+ YEARS AGO. SURGEON USED LONG AR15 NECK WITH BLOBALL HEAD AND STRYKER CUP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
130126 ANCA FIT LINER LINER LPH HRY NI

Patients

Seq Age Sex Outcome Treatment
1 75 YR Required Intervention