FDA Adverse Event Injury Summary report: N

KONIG MOGEN CLAMP

MDR report key: 23679962 · Received December 1, 2025

Report

Report Number
MW5179566
Event Type
Injury
Date Received
December 1, 2025
Date of Event
October 3, 2025
Report Date
November 21, 2025
Manufacturer
MEDLINE INDUSTRIES, LP - NORTHFIELD
Product Code
HFX
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
KY, US
Reporter Occupation
RISK MANAGER
Health Professional
Yes

Narratives

Description of Event or Problem · 0

DURING CIRCUMCISION PROCEDURE, CLAMP MALFUNCTIONED, LACERATING THE FORESKIN ALL THE WAY DOWN TO THE SCROTUM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2054026 KONIG MOGEN CLAMP CLAMP, CIRCUMCISION HFX MEDLINE INDUSTRIES, LP - NORTHFIELD MDS 9900025K

Patients

Seq Age Sex Outcome Treatment
1 1 DA Male Hospitalization| R