OptiMesh Multiplanar Expandable Interbody Fusion System 33-09-14Recalls & reported problems
Spineology Inc. · Graft Tube · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M7403120056), received between Aug 27, 2024 and Aug 27, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Improper or Incorrect Procedure or Method1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 27, 2024Improper or Incorrect Procedure or Method; Detachment of Device or Device Component; Improper or Incorrect Procedure or Method; Detachment of Device or Device Component
THE PATIENT UNDERWENT AN INTERBODY FUSION PROCEDURE ON (B)(6) 2024. DURING THE SURGICAL PROCEDURE, MALLET IMPACT FORCES WERE APPLIED TO DEPLOY BONE GRAFT MATERIAL THROUGH THE GRAFT TUBE INSTRUMENT CAUSING THE GRAFT TUBE SHAFT TO DETACH FROM THE GRAFT TUBE FUNNEL HEAD. UPON FURTHER IMPACTION, THE SHAFT COMPONENT INADVERTENTLY ADVANCED VENTRAL TO THE ANTERIOR ANNULUS. THE SHAFT COMPONENT WAS RETRIEVED AND THE SURGEON CONFIRMED NO PATIENT INJURY OR CONSEQUENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20081190 ↗
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- R3 71364450Smith & Nephew, Inc. · ORTHOPEDIC MANUAL SURGICAL INSTRUMENT520 reports
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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