VuMesh™ 15-10-1215Recalls & reported problems
Seaspine Orthopedics Corporation · 12mm Sq Cage X 15mm Long · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10889981036225), received between Sep 27, 2023 and Sep 4, 2024 — classified as 2 malfunctions.
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
- Material Separation1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 4, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
ON (B)(6) 2024, A PATIENT UNDERWENT SPINAL SURGERY CONSISTING OF SEASPINE'S VUMESH VERTEBRAL BODY REPLACEMENT SYSTEM. X-RAYS TAKEN THE SAME DAY SHOW THAT THE CAGE'S TANTALUM MARKER HAD MIGRATED OUTSIDE OF THE CAGE. MULTIPLE ATTEMPTS FOR ADDITIONAL INFORMATION WERE MADE. NO RESPONSE WAS RECEIVED. IT IS UNKNOWN IF THE CAGE REMAINS IMPLANTED. NO PATIENT INJURY WAS REPORTED.
Patient problems: Insufficient Information
MAUDE report 20135493 ↗MalfunctionSep 27, 2023Material Separation; Material Separation
A PATIENT RECENTLY UNDERWENT SPINAL SURGERY IN WHICH SEASPINE'S VUMESH VERTEBRAL BODY REPLACEMENT SYSTEM WAS UTILIZED. ON (B)(6) 2023. EASPINE WAS NOTIFIED THAT DURING A STANDARD FOLLOW-UP X-RAY, IT WAS DETECTED THAT A TANTALUM MARKER/BEAD HAD BECOME DETACHED FROM THE VUMESH INTERBODY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17827002 ↗
Other SPINAL VERTEBRAL BODY REPLACEMENT DEVICE devices
- GIZA Corpectomy implant Giza, Diam 14 mm, 23-32 mm, 7-10 DegEden Spine Europe SA · Spinal Vertebral Body Replacement Device1 recall0 reports
- X-CORE 7160012Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7220018Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7160014Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7180018Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- X-CORE 7180016Nuvasive, Inc. · SPINAL VERTEBRAL BODY REPLACEMENT DEVICE1 recall0 reports
- GIZA Corpectomy implant Giza, Diam 14 mm, 18-22 mm, 2-5 DegEden Spine Europe SA · Spinal Vertebral Body Replacement Device1 recall0 reports
- GIZA Corpectomy implant Giza, Diam 14 mm, 23-32 mm, 2-5 DegEden Spine Europe SA · Spinal Vertebral Body Replacement Device1 recall0 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page