SURGIFY MEDICAL OY recalls Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines & accessories (simple, powered

Recalled July 1, 2026 · FDA recall Z-2557-2026 · SURGIFY MEDICAL OY

Hazard

Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS). · FDA Class II

Units

N/A

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, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; 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 →