FDA Adverse Event Injury Summary report: N

MCKESSON BRANDS

MDR report key: 23990722 · Received January 7, 2026

Report

Report Number
1451040-2026-00001
Event Type
Injury
Date Received
January 7, 2026
Date of Event
November 24, 2025
Report Date
January 7, 2026
Manufacturer
CONOD MEDICAL CO., LTD
Product Code
PYE
UDI-DI
10612479205892
Adverse Event
Yes
Product Problem
Yes
Report Source
Distributor report
Reporter Location
FL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Description of Event or Problem · 0

IT WAS REPORTED BY THE CUSTOMER THAT WHEN ATTEMPTING TO REMOVE STAPLE, THE PLIERS CRIMPED THE STAPLE AND PUSHED IT DOWNWARD INTO THE SKIN INSTEAD OF LIFTING IT OUTWARD. PATIENT DID HAVE TO GO INTO SURGEON'S OFFICE TO GET THE STAPLES REMOVED AFTER THEY BECAME BOWED AND REMAINED IN THE SKIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
50238 MCKESSON BRANDS STAPLE REMOVER TRAY, SKIN W/PREP PYE CONOD MEDICAL CO., LTD CZE06-02 10612479205892

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention