Surgify Medical Oy: Drills, Burrs, Trephines & Accessories (simple, Powered)
Recall Summary Surgify Medical is recalling Surgify Halo 4.0 mm Short burrs (Model 40.070.NVG.H1) and related drilling accessories used in spinal surgery because they may break during use. The affected products were distributed nationwide to hospitals and surgical facilities. This is a Class II recall, meaning the product could cause serious injury but is not expected to cause death.
- Recalling firm
- SURGIFY MEDICAL OY
- Product
- Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.H1; 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/542f0e36-fe3b-47b0-a3f0-f84713720dcd