Surgify Medical Oy: Drills, Burrs, Trephines & Accessories (simple, Powered)
Surgify Halo Drill Burr Recall Summary Surgify Medical is recalling Surgify Halo 3.0mm Long drill burrs (Model 30.125.NVG.U2) used in spinal surgery because the burrs may break during use. The burrs were distributed nationwide to hospitals and surgical facilities. Patients who had bi-portal endoscopic spinal surgery using this product may have been affected.
- Recalling firm
- SURGIFY MEDICAL OY
- Product
- Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines & accessories (simple, powered)
- Reason
- Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-04-30
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution in the states of MN, MA, IN, LA, CA, NY, FL.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ee4f576d-e9f8-41f8-abd7-890ba4678030