Surgify Medical Oy: Drills, Burrs, Trephines & Accessories (simple, Powered)
Recall Summary Surgify Medical is recalling certain Halo surgical burrs (model 40.125.NVG.U1) used in spinal surgery because they may break during use. The burrs were distributed nationwide to hospitals and surgical facilities. Patients who underwent bi-portal endoscopic spinal surgery (BESS) using these burrs may be affected.
- Recalling firm
- SURGIFY MEDICAL OY
- Product
- Surgify Halo, 40 mm, Long, Model/Catalog Number: 40.125.NVG.U1; 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/60d62c73-a5ae-4a66-81dc-e68ed0edabd1