FDA Adverse Event Injury Summary report: N

RIBLOC U PLUS 75MM RIB PLATE

MDR report key: 5881001 · Received August 16, 2016

Report

Report Number
3005670412-2016-00009
Event Type
Injury
Date Received
August 16, 2016
Date of Event
July 8, 2016
Report Date
August 16, 2016
Manufacturer
ACUTE INNOVATIONS, LLC
Product Code
HRS
UDI-DI
10814493010388
PMA / PMN Number
K113318
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IN (B)(6) 2016, FIVE RIB PLATES WERE SUCCESSFULLY IMPLANTED TO TREAT RIB FRACTURES. THE PATIENT DEVELOPED AN INFECTION AND ALL FIVE PLATES WERE REMOVED ON (B)(6) 2016. PLATES WERE NOT RETURNED FOR INVESTIGATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
532898 RIBLOC U PLUS 75MM RIB PLATE PLATE, FIXATION, BONE HRS ACUTE INNOVATIONS, LLC RBL1302 10814493010388

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention