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SURGIFY MEDICAL OY recalls Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.H1; drills, burrs, trephines & accessories (simple, p
Recalled July 1, 2026 · FDA recall Z-2564-2026 · SURGIFY MEDICAL OY
Hazard
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). · FDA Class II
Units
53 units
Sold at
US Nationwide distribution in the states of MN, MA, IN, LA, CA, NY, FL.
Description
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Product
Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered)
Manufacturer(s)
SURGIFY MEDICAL OY
Made in
Finland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →