FDA Adverse Event Injury Summary report: N

PLATE, FIXATION, BONE

MDR report key: 9527103 · Received December 27, 2019

Report

Report Number
3025141-2019-00695
Event Type
Injury
Date Received
December 27, 2019
Report Date
December 23, 2019
Manufacturer
ACUMED LLC
Product Code
HRS
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL MDRS ASSOCIATED WITH THIS ARTICLE: 3025141-2019-00696: CASE 2, 3025141-2019-00697: CASE 3.

Description of Event or Problem · 1

ARTICLE: DISPLACED MIDSHAFT CLAVICLE FRACTURE IN ATHLETES - SHOULD WE OPERATE?; DE SOUZA, NEYDSON ANDRE SOLPOSTO MARQUES; BELANGERO, PAULO SANTORO; DE FIGUEIREDO, EDUARDO ANTONIO; POCHINI, ALBERTO DE CASTO; ANDREOLI, CARLOS VICENTE; EJNISMAN, BENNO; REV BRAS ORTOP, 2018; 53(2): 171-175. CASE 1: PATIENT'S BROKEN CLAVICLE WAS TREATED BY IMPLANTING AN ACUMED MIDSHAFT CLAVICLE PLATE. PATIENT EXPERIENCED LOSS IN SENSATION, MINIMIZED BY DISSECTION OF THE SUPRACLAVICULAR NERVE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1320411 PLATE, FIXATION, BONE HRS ACUMED LLC

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention