EXPEDIUM 179702525Recalls & reported problems
Medos International Sàrl · EXPEDIUM SPINE SYSTEM MONOAXIAL SCREW 5.5 x 5 x 25mm · Class 2 · Implant
All models of EXPEDIUM (291)
Data updated Oct 16, 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 10705034064673), received between Feb 24, 2026 and Mar 9, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (2 reports).
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Twisted/Bent2
- Device-Device Incompatibility1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 9, 2026Device-Device Incompatibility; Material Twisted/Bent
IT WAS REPORTED THAT PATIENT UNDERWENT POSTERIOR SPINAL FUSION (T3) FOR AIS ON (B)(6) 2025. THE SET SCREW WAS PLACED DURING SURGERY, AND WHEN THE SURGEON TRIED TO LOOSEN IT FOR CORRECTIVE PURPOSES, IT SPUN FREELY AND COULD NOT BE LOOSENED. UPON REMOVING THE SCREW AND CHECKING, IT WAS FOUND THAT THE THREADS ON THE SET SCREW WERE DAMAGED. THE SCREW WAS REPLACED AND A NEW SET SCREW WAS USED. THE SURGERY WAS COMPLETED SUCCESSFULLY WITH NO DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24547801 ↗MalfunctionFeb 24, 2026Material Twisted/Bent
IT WAS REPORTED THAT PATIENT UNDERWENT A POSTERIOR SPINAL FUSION FOR IDIOPATHIC SCOLIOSIS ON (B)(6) 2026. AFTER THE SET SCREW WAS INSTALLED, THE SCREWDRIVER SPUN FREELY, MAKING IT IMPOSSIBLE TO TIGHTEN OR REMOVE THE SET SCREW, SO THE SURGEON DECIDED TO REMOVE AND REPLACE EACH SCREW. THE SURGERY WAS COMPLETED SUCCESSFULLY WITHIN THIRTY MINUTES OF DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24429155 ↗
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- ZEVO™ Anterior Cervical Plate System 7710015Medtronic Sofamor Danek, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 recall1 report
- Mariner RDX MX1-000040Seaspine Orthopedics Corporation · Appliance, fixation, spinal intervertebral body1 recall0 reports
- Mariner RDX MX1-000030Seaspine Orthopedics Corporation · Appliance, fixation, spinal intervertebral body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430112Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- Elegance® Anterior Cervical Plate 53430224Clariance · Appliance, Fixation, Spinal Intervertebral Body1 recall0 reports
- XLP 7565050Nuvasive, Inc. · APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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