Class II
Medical Device Recall: Surgify Halo, 40 mm, Long, Model/Catalog Number: 40.125.NVG.U1; drills, burrs, trephines & accessories (simple, powered)
SURGIFY MEDICAL OY · April 30, 2026
Reason for Recall
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Distribution
US Nationwide distribution in the states of MN, MA, IN, LA, CA, NY, FL.
States Affected
NATIONWIDE
Quantity Affected
0
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2563-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.