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VuePoint 8976240Recalls & reported problems

Nuvasive, Inc. · VuePoint® II Rod, 240mm 45° Precurved · Class 2 · Implant

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 00887517137562), received between Jan 14, 2016 and Jan 14, 2016 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Fracture1
  • Loose or Intermittent Connection1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 14, 2016Fracture; Loose or Intermittent Connection

    FOLLOWING IMPLANTATION OF A POSTERIOR CERVICAL FIXATION CONSTRUCT ON (B)(6) 2015, FRACTURE OF A ROD AND A KEEL PLATE SCREW LOOSENING WAS REPORTED. NO PATIENT INJURY HAS BEEN REPORTED. REVISION OF THE CONSTRUCT WAS REPORTED TO HAVE OCCURRED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 5368571 ↗

Other APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices

All APPLIANCE, FIXATION, SPINAL INTERLAMINAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.