FDA Adverse Event Malfunction Summary report: N

JUSTRIGHT 5MM STAPLER

MDR report key: 19248393 · Received May 6, 2024

Report

Report Number
19248393
Event Type
Malfunction
Date Received
May 6, 2024
Date of Event
March 4, 2024
Report Date
March 4, 2024
Manufacturer
BOLDER SURGICAL, LLC
Product Code
GAG
Product Problem
Yes
Report Source
User Facility report
Reporter Location
OH
Reporter Occupation
RISK MANAGER
Health Professional
N

Narratives

Description of Event or Problem · 0

JUSTRIGHT 5MM STAPLER MISFIRED DURING SURGICAL CASE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
591841 JUSTRIGHT 5MM STAPLER STAPLER, SURGICAL GAG BOLDER SURGICAL, LLC JR-ST25-2.0 75HC5678

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown