ARROW
Received Jan 21, 2026 · Event occurred Dec 15, 2025
Report 24130262 · MDR key 24130262
Device
Generic name
Catheter, Hemodialysis, Non-implanted
Manufacturer
Teleflex IncorporatedCatalog number
AK-25142-CDC
Lot number
33F25E0086
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
PLACING A LEFT FEMORAL VEIN QUINTON CATHETER, WAS ABLE TO CANNULATE THE VEIN IMMEDIATELY ON FIRST STICK AND THREAD THE GUIDEWIRE WITHOUT DIFFICULTY. AFTER CONFIRMING THE GUIDEWIRE WAS APPROPRIATELY POSITIONED IN THE VEIN, WAS ABLE TO DILATE WITHOUT DIFFICULTY. WAS ABLE TO THREAD THE CATHETER OVER THE GUIDEWIRE, HOWEVER WHEN PROVIDER WENT TO REMOVE THE GUIDEWIRE, PROVIDER NOTICED THAT THE GUIDEWIRE WAS SHEARED AND UNRAVELED IN PLACES. IN ORDER TO ENSURE THE ENTIRE GUIDEWIRE WAS REMOVED EN BLOC, I REMOVED THE CATHETER AND THE ENTIRE GUIDEWIRE. I INSPECTED THE GUIDEWIRE WITH TELEICU ATTENDING. J LOOP INTACT. END OF GUIDEWIRE INTACT. THERE ARE AREAS OF THE GUIDEWIRE THAT ARE UNRAVELED ALONG THE LENGTH. I HAVE SAVED THE ENTIRE GUIDEWIRE AND THE CATHETER FOR REVIEW.