Surgify Medical recalls Halo spinal surgery tools due to potential burr breakage during BESS procedures. Affected items include specific model and lots; check your product details to determine if recalled.
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Surgify Medical is recalling their Halo spinal surgery tools (model 40.070.NVG.H1) because burrs could break during spinal surgery. This risk could lead to complications if the burr breaks during a procedure.
During bi-portal endoscopic spinal surgery, the burr could break, potentially causing injury to the surgical site. This risk occurs when the burr is used in the specific procedure that requires precise cutting.
Surgical teams using the Surgify Halo 4.0mm Short model for spinal procedures are most at risk. Patients undergoing bi-portal endoscopic spinal surgery (BESS) may be affected if the tool is used.
Check for the model number 40.070.NVG.H1 on the Surgify Halo 4.0mm Short tool. The recall covers all lots until the manufacturer updates the instructions for use.
Look for the model number 40.070.NVG.H1 on the Surgify Halo 4.0mm Short tool to confirm if it's affected.
This recall affects surgical teams using the Surgify Halo tools during spinal procedures, not patients directly.
Check for the model number 40.070.NVG.H1 on the Surgify Halo 4.0mm Short tool. The recall covers all lots until the manufacturer updates the instructions for use.
No immediate stop is required, but surgical teams should check if their tools are affected and follow the manufacturer's update process.
We’ve drafted a message you can send Surgify Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2560-2026 — Surgify Medical Surgify Medical Hello, I own a Surgify Medical that is covered by recall Z-2560-2026 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.
