MAUDE Adverse Event Report: MEDLINE INDUSTRIES, LP - NORTHFIELD MOGEN; CLAMP, CIRCUMCISION

Model Number MARINA

Patient Problem Hemorrhage/Bleeding (1888)

Event Date 02/01/2024

Event Type  malfunction  

Event Description

Mogen clamp cut the foreskin instead of clamping it which allowed for excessive bleeding and need for intervention.

• Brand Name: MOGEN
• Type of Device: CLAMP, CIRCUMCISION
• Manufacturer (Section D): MEDLINE INDUSTRIES, LP - NORTHFIELD
• MDR Report Key: 18922087
• MDR Text Key: 338145626
• Report Number: MW5152917
• Device Sequence Number: 1
• Product Code: HFX
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Nurse
• Type of Report: Initial
• Report Date: 03/13/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/15/2024
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: MARINA
• Is the Reporter a Health Professional?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Other
• Patient Age: 2 DA
• Patient Sex: Male
• Patient Ethnicity: Non Hispanic
• Patient Race: White