Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.H1; drills, burrs, trephines & accessories (simple, powe... — FDA record Z-2570-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 30, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.H1; drills, burrs, trephines & accessories (simple, powered)
Reason
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Classification
Class II
Recalling firm
SURGIFY MEDICAL OY
Quantity
N/A
Agency-reported status
Ongoing
Source record identifier
Z-2570-2026

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityUDI: 06429811532106 ; All lots until the IFU update has been implemented

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide distribution in the states of MN, MA, IN, LA, CA, NY, FL.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jul 1, 2026
Recall initiation date
Apr 30, 2026
Center classification date
Jun 24, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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