FDA Adverse Event Malfunction Summary report: N

KIT: CIRCUMCISION 20/CS

MDR report key: 25144926 · Received May 11, 2026

Report

Report Number
1030451-2026-00013
Event Type
Malfunction
Date Received
May 11, 2026
Date of Event
April 24, 2026
Report Date
May 11, 2026
Manufacturer
MEDICAL ACTION INDUSTRIES
Product Code
OHG
UDI-DI
20809160006020
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NV, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

INCIDENT 2 OF 5 THE PRODUCT INVOLVED IN THE EVENT IS NOT AVAILABLE FOR EVALUATION. A FOLLOW-UP REPORT WILL BE PROVIDED UPON CONCLUSION OF INVESTIGATION. MEDICAL ACTION INDUSTRIES IS THE MANUFACTURER OF THE CIRCUMCISION CONVENIENCE KIT CONTAINING THE COMPLAINT STRAIGHT HEMOSTAT COMPONENT, R0598 (LOTS 2541R0598 & 2441R0598G). THE TWO LOTS MANUFACTURED IN THE COMPLAINT CONVENIENCE KIT LOT WERE SOURCED FROM TWO DIFFERENT SUPPLIERS, GLOBAL INSTRUMENTS INC. (FDA REGISTRATION 1057200) & TAMZON INSTRUMENTS, INC. (FDA REGISTRATION 1421530). THIS PRODUCT INCIDENT IS DOCUMENTED IN THE COMPLAINT DATABASE AND IDENTIFIED AS COMPLAINT (B)(4). THIS INFORMATION IS SUBMITTED PURSUANT TO 21CFR803, IN COMPLIANCE WITH THE MEDICAL DEVICE REPORTING REQUIREMENT AND SHOULD NOT BE CONSIDERED TO BE AN ADMISSION THAT PRODUCT IS DEFECTIVE OR HAS CAUSED SERIOUS INJURY.

Description of Event or Problem · 0

STRAIGHT HEMOSTAT BROKE DURING CIRCUMCISION PROCEDURE. THE HEMOSTAT INSTRUMENT FAILED TO HOLD THE SKIN, COMING LOOSE. NO PATIENT HARM RESULTED FROM INCIDENT. SITE REPORTED THE HEMOSTAT FAILED 4-5 TIMES DURING 19 TOTAL CIRCUMCISIONS PERFORMED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
217374 KIT: CIRCUMCISION 20/CS KIT: CIRCUMCISION 20/CS OHG MEDICAL ACTION INDUSTRIES 56779 340235 20809160006020

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown