FDA Adverse Event Malfunction Summary report: N

WECK

MDR report key: 24208189 · Received January 29, 2026

Report

Report Number
24208189
Event Type
Malfunction
Date Received
January 29, 2026
Date of Event
January 23, 2025
Report Date
January 20, 2026
Manufacturer
TELEFLEX, LLC
Product Code
HAO
Product Problem
Yes
Report Source
User Facility report
Reporter Location
AZ
Reporter Occupation
RISK MANAGER
Health Professional
N

Narratives

Description of Event or Problem · 0

PER STAFF, FINAL CLOSING COUNT PERFORMED AT 1205. SCRUB TECH INFORMED NURSE THAT 4/6 FISH HOOKS HAD BROKEN/SNAPPED, AND THE CURVED METAL HOOK WAS MISSING ON 2/6 FISH HOOKS. SURGEON NOTIFIED. ONE METAL HOOK LOCATED DURING END OF COUNT. UNABLE TO LOCATE ONE HOOK. SURGEON REQUESTED RADIOLOGY. X-RAY OF HEAD TAKEN AND HOOK VISUALIZED. SURGEON ATTEMPTED TO REMOVE HOOK, BUT UNABLE TO LOCATE, EVEN AFTER MULTIPLE X-RAYS AND ATTEMPTS TO REMOVE. HOOK DIFFICULT TO LOCATE IN PART DUE TO PATIENT HEAD IN METAL MAYFIELD HOLDER. SURGEON CLOSED INCISION IN ORDER TO REMOVE MAYFIELD. PATIENT RE-PREPPED AND DRAPED, AND NEW X-RAYS TAKEN WITH CONTINUOUS ATTEMPTS TO REMOVE HOOK. HOOK REMOVED BY SURGEON AND FINAL CLOSING COUNT PERFORMED, COUNT CORRECT. BROKEN FISH HOOKS COLLECTED AND GIVEN TO NURSE SUPERVISOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
272176 WECK INSTRUMENT, SURGICAL, NON-POWERED HAO TELEFLEX, LLC 73G2400214, 73G2400158

Patients

Seq Age Sex Outcome Treatment
1 41 YR Unknown