Spineology recalls Graft Tube surgical instruments due to possible detachment risk when not used per surgical technique. Affected units have specific lot numbers and catalog codes.
Possible detachment of the Graft Tube shaft from the Graft Tube funnel head when it is not used as instructed by our surgical technique.
Spineology is recalling Graft Tube surgical instruments that could detach from the funnel head if not used exactly as instructed in their surgical technique guide. This poses a risk of injury during surgery if the detachment occurs.
The Graft Tube shaft may detach from the funnel head if the instrument isn't used according to Spineology's surgical technique guide. This could lead to the graft material being misplaced during spinal surgery, potentially causing injury to the patient.
Surgical teams using Spineology's Graft Tube instruments for spinal procedures. Patients undergoing surgery with this specific instrument are at risk if the detachment happens during the procedure.
Check for lot numbers CH20003 or BE22003 on the instrument. The catalog number is 312-0056 and part number is 33-09-14. The instrument is used in spinal surgery to deploy graft material.
Ensure the Graft Tube is used exactly as instructed in Spineology's Surgical Technique Guide to prevent shaft detachment from the funnel head.
The Graft Tube is safe when used exactly as instructed in Spineology's Surgical Technique Guide. Improper use could cause detachment.
Lot numbers CH20003 and BE22003 are affected.
Check for lot numbers CH20003 or BE22003, catalog number 312-0056, and part number 33-09-14 on the instrument.
We’ve drafted a message you can send Spineology to request your refund or repair — edit it as you like.
Subject: Recall Z-0117-2025 — Spineology Spineology Hello, I own a Spineology that is covered by recall Z-0117-2025 from Spineology. 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.
