FDA Adverse Event Injury Summary report: N

RIBLOC U PLUS 50MM RIB PLATE

MDR report key: 5880990 · Received August 16, 2016

Report

Report Number
3005670412-2016-00006
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
10814493010371
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
533026 RIBLOC U PLUS 50MM RIB PLATE PLATE, FIXATION, BONE HRS ACUTE INNOVATIONS, LLC RBL1301 10814493010371

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention