FDA Adverse Event Injury Summary report: N

BIA400 IMPLANT 4MM W ABUTMENT 10MM

MDR report key: 9589617 · Received January 14, 2020

Report

Report Number
6000034-2020-00011
Event Type
Injury
Date Received
January 14, 2020
Report Date
December 30, 2019
Manufacturer
COCHLEAR BONE ANCHORED SOLUTIONS AB
Product Code
MAH
UDI-DI
09321502022385
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
OH, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THIS REPORT IS SUBMITTED ON JANUARY 15, 2020.

Description of Event or Problem · 1

PER THE CLINIC, THE PATIENT EXPERIENCED AN INFECTION AT THE ABUTMENT SITE THAT WAS TREATED WITH ORAL ANTIBIOTICS. THE IMPLANT REMAINS IN-SITU.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
49198 BIA400 IMPLANT 4MM W ABUTMENT 10MM COCHLEAR BAHA CONNECT SYSTEM MAH COCHLEAR BONE ANCHORED SOLUTIONS AB 93331 COH1280934 09321502022385

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention