Surgify Medical recalls Halo spinal surgery tools (model 40.125.NVG.H1) due to potential burr breakage during BESS procedures. Affected items include drills, burrs, and trephines. All units until IFU update are recalled.
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Surgify Medical is recalling specific spinal surgery tools (Halo 4.0mm Short model 40.125.NVG.H1) because burrs might break during spinal surgery. This could lead to complications for patients undergoing bi-portal endoscopic spinal procedures.
During spinal surgery using the Halo tools, burrs could break unexpectedly. This breakage might cause tissue damage or other complications during the procedure. The hazard occurs specifically in bi-portal endoscopic spinal surgery (BESS).
Surgical teams using the recalled Halo tools for bi-portal endoscopic spinal surgery (BESS) are most at risk. Patients undergoing these procedures with the affected tools may face complications.
Check for the model number 40.125.NVG.H1 on the Surgify Halo 4.0mm Short tools. The recall covers all units until the manufacturer updates the instructions for use (IFU).
Look for the model number 40.125.NVG.H1 on the Surgify Halo 4.0mm Short tools.
Reach out to Surgify Medical for guidance on next steps after identifying the affected product.
The recall is due to potential burr breakage during bi-portal endoscopic spinal surgery (BESS), which could cause complications for patients.
The affected products are Surgify Halo 4.0mm Short tools with model number 40.125.NVG.H1, including drills, burrs, trephines, and accessories.
Check for the model number 40.125.NVG.H1 on the Surgify Halo 4.0mm Short tools. The recall covers all units until the manufacturer updates the instructions for use.
We’ve drafted a message you can send Surgify Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2562-2026 — Surgify Medical Surgify Medical Hello, I own a Surgify Medical that is covered by recall Z-2562-2026 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.
