Surgify Medical recalls Halo spinal surgery tools (model 54.070.NVG.U1) due to potential burr breakage during BESS procedures. Affected items include drills, burrs, trephines. No remedy specified in recall notice.
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Surgify Medical is recalling specific spinal surgery tools (Halo 5.4mm Short model 54.070.NVG.U1) because they could break during spinal surgery, potentially causing injury. This recall affects surgeons and medical staff using these tools in bi-portal endoscopic spinal procedures.
The recalled burrs and tools could break during spinal surgery, which might lead to tissue damage or other complications. This risk occurs specifically during bi-portal endoscopic spinal procedures (BESS) where the tools are used.
Surgeons and medical staff who use the recalled Halo spinal tools during bi-portal endoscopic spinal surgery (BESS) are most at risk. Patients undergoing these procedures with the affected tools could face complications.
Check for the model number 54.070.NVG.U1 on the Surgify Halo 5.4mm Short tools. The recall covers all items until the manufacturer updates the instructions for use (IFU).
Look for the model number 54.070.NVG.U1 on the Surgify Halo 5.4mm Short tools or accessories.
The recall notice does not specify any remedy or fix for burr breakage.
Check for the model number 54.070.NVG.U1 on the Surgify Halo 5.4mm Short tools or accessories. The recall covers all items until the manufacturer updates the instructions for use.
The recall does not specify a stop-use instruction, so users should check if their tools are affected before taking action.
We’ve drafted a message you can send Surgify Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2567-2026 — Surgify Medical Surgify Medical Hello, I own a Surgify Medical that is covered by recall Z-2567-2026 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.
