Vital MIS Spinal Fixation System 07.02100.001Recalls & reported problems
Highridge Medical, LLC · Rod Gripper · 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 03662663126014), received between Mar 25, 2026 and Mar 25, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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
- Fracture1
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.
MalfunctionMar 25, 2026Fracture
IT WAS REPORTED THAT ONE OF THE SCREWS/PEGS AT THE TIP OF A VITALITY ROD GRIPPER FRACTURED INTRA-OP, AND THAT THE PIECE BROKE WHILE UNDER STRESS AFTER BEING SECURED TO A ROD IN THE THORACIC SPINE. THE PIECE WAS RETRIEVED, AND A SECONDARY DEVICE WAS AVAILABLE TO USE FOR THE REST OF THE PROCEDURE. THERE WAS NO PATIENT OR PROCEDURAL IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24689350 ↗
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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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