Surgify Medical recalls Halo 3.0mm Short surgical instruments due to potential burr breakage during spinal procedures. Affected models include specific catalog numbers and lots until IFU update.
Potential for burr breakage, occurring during bi-portal endoscopic spinal surgery (BESS).
Surgify Medical is recalling their Halo 3.0mm Short surgical instruments because they might break during spinal surgery, which could cause injury. This affects specific models and lots until the manufacturer updates their instructions.
The burrs in these instruments could break during spinal surgery, potentially causing injury to the patient. This risk occurs specifically during bi-portal endoscopic spinal procedures (BESS), where the instruments are used to create small openings in the spine.
Surgical teams using the specific model and lots of Surgify Halo instruments are most at risk during bi-portal endoscopic spinal procedures. Patients undergoing such surgeries may be affected if the instruments are used without the updated instructions.
Check for the model number 30.070.NVG.U2 on the Surgify Halo 3.0mm Short instruments. The recall covers all lots until the manufacturer implements the updated instructions.
Look for the model number 30.070.NVG.U2 on the Surgify Halo 3.0mm Short instruments.
The recall covers all lots until the manufacturer implements the updated instructions.
The recall is due to potential burr breakage during bi-portal endoscopic spinal surgery, which could cause injury.
The Surgify Halo 3.0mm Short model with catalog number 30.070.NVG.U2, including drills, burrs, trephines, and accessories.
No, but you should wait for the manufacturer's updated instructions before using them.
We’ve drafted a message you can send Surgify Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2556-2026 — Surgify Medical Surgify Medical Hello, I own a Surgify Medical that is covered by recall Z-2556-2026 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.
