Surgify Medical recalls Halo 4.0mm short surgical instruments due to potential burr breakage during spinal procedures. Affected models include 40.070.NVG.U1 with UDI 06429811532267. 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 instruments that could break during procedures, potentially causing injury. This recall affects instruments used in bi-portal endoscopic spinal surgery (BESS) and requires immediate attention from medical professionals.
The instruments could break during spinal surgery procedures, which might lead to complications such as tissue damage or bleeding. This risk occurs specifically when using the instruments in bi-portal endoscopic spinal surgery (BESS) techniques.
Medical professionals using the recalled Surgify Halo instruments for spinal surgery are most at risk. The recall applies to specific models sold with the UDI number 06429811532267.
Check for the model number 40.070.NVG.U1 on the Surgify Halo instruments. The recall covers all units until the manufacturer implements the updated instructions for use (IFU).
Verify the model number on the instrument to confirm if it matches 40.070.NVG.U1.
The recall notice does not specify any remedy or fix for the burr breakage issue.
The recall affects bi-portal endoscopic spinal surgery (BESS) procedures where the instruments are used.
Check the model number on the instrument; if it is 40.070.NVG.U1, it is part of the recall.
We’ve drafted a message you can send Surgify Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2561-2026 — Surgify Medical Surgify Medical Hello, I own a Surgify Medical that is covered by recall Z-2561-2026 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.
