Surgify Medical recalls Halo 40mm drills for potential burr breakage during spinal surgery. Affected models include 40.125.NVG.U1. No remedy stated in official notice.
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Surgify Medical is recalling Halo 40mm surgical drills that may break during spinal surgery. This could lead to complications if burrs fracture during procedures. The recall covers specific model numbers and all units until a fix is implemented.
Burr breakage during spinal surgery could cause tissue damage or complications. The hazard occurs when the drills are used in bi-portal endoscopic spinal surgery (BESS) procedures. This risk is specific to the surgical context and not typical for regular use.
Surgical teams using the Surgify Halo 40mm drills for spinal procedures are most at risk. Patients undergoing bi-portal endoscopic spinal surgery (BESS) may be affected if the drills break during the procedure.
Check for the model number 40.125.NVG.U1 on the Surgify Halo 40mm drills. The recall covers all units until the manufacturer updates the instructions for use.
Look for the model number 40.125.NVG.U1 on the Surgify Halo 40mm drills.
The official recall notice does not state any remedy or fix for the burr breakage issue.
Check for the model number 40.125.NVG.U1 on the Surgify Halo 40mm drills. The recall covers all units until the manufacturer updates the instructions for use.
The recall notice does not specify a stop-use instruction, so there is no immediate action required beyond checking the model number.
We’ve drafted a message you can send Surgify Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2563-2026 — Surgify Medical Surgify Medical Hello, I own a Surgify Medical that is covered by recall Z-2563-2026 from Surgify Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
