Surgify Medical recalls Halo surgical instruments due to potential burr breakage during spinal surgery. Affected models include 5.4mm Short with catalog number 54.070.NVG.H1. All units until IFU update are included.
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Surgify Medical is recalling specific spinal surgery instruments (Halo 5.4mm Short model 54.070.NVG.H1) because they may break during spinal surgery, causing injury. This recall affects surgeons and hospitals using these tools.
The surgical instruments may break during spinal surgery procedures, potentially causing injury to patients. This breakage risk occurs specifically in bi-portal endoscopic spinal surgery (BESS) techniques.
Surgeons and hospitals using the Surgify Halo 5.4mm Short model 54.070.NVG.H1 for spinal procedures are most at risk. The recall covers all units until the manufacturer updates the instructions.
Check for the model number 54.070.NVG.H1 on the Surgify Halo 5.4mm Short instruments. The recall includes all units until the manufacturer updates the instructions.
Look for the model number 54.070.NVG.H1 on the Surgify Halo 5.4mm Short instruments.
The Surgify Halo instruments may break during spinal surgery, specifically in bi-portal endoscopic spinal surgery (BESS), which could cause injury.
The recall covers all units until the manufacturer updates the instructions. Check the model number to confirm if your instrument is affected.
Yes, burr breakage during spinal surgery could cause injury to patients, which is why this product is being recalled.
We’ve drafted a message you can send Surgify Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2566-2026 — Surgify Medical Surgify Medical Hello, I own a Surgify Medical that is covered by recall Z-2566-2026 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.
