MalfunctionNFA
SPIDERFX 4MM
Received Jun 25, 2026 · Event occurred Feb 2, 2026
Report 25619659 · MDR key 25619659
Device
Generic name
Temporary Coronary Saphenous Vein Bypass Graft For Embolic Protection
Manufacturer
MedtronicModel number
SPD2-US-040-320Lot number
C177213
Patient
NA · Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
MEDTRONIC SPIDER FILTER WOULD NOT RETRACK IN TO IT'S SHEATH. UNABLE TO USE PRODUCT PER CATHETER DEFECT. NOT USED ON PATIENT.