MalfunctionFOZ
MIDLINE GUIDEWIRE
Received Jul 14, 2026 · Event occurred Jul 4, 2026
Report MW5190730 · MDR key 25816820
Device
Generic name
Catheter, Intravascular, Therapeutic, Short-term Less Than 30 Days
Manufacturer
Bard Access Systems, Inc.Model number
F118088PTLot number
RELP1372
Patient
NA · Unknown
- Insufficient Information
Narrative
Description of Event or Problem
A 18G 8 CM MIDLINE GUIDEWIRE TESTED PRIOR TO INSERTION AND WHEN DEPLOYING THE GUIDEWIRE, IT DID NOT DEPLOY. APPEARS TO BE STUCK INSIDE DEVICE. DID NOT REACH PATIENT.