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VuePoint 8980018P3Recalls & reported problems

Nuvasive, Inc. · VuePoint II Screw/Set Screw, 3.5x18mm MA · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517826367), received between Jun 26, 2019 and Jun 26, 2019 — classified as 1 injury.

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

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Numbness1

Recent adverse event reports

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

  • InjuryJun 26, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    ON (B)(6) 2019, PATIENT UNDERWENT A POSTERIOR CERVICAL SPINAL FUSION PROCEDURE AT C4/5/6 LEVELS WITH NO REPORTED ISSUE. ON (B)(6) 2019, ONE DAY POSTOPERATIVE, THE PATIENT STARTED TO EXPERIENCE NUMBNESS IN RIGHT UPPER LIMB. THAT SAME DAY THE PATIENT UNDERWENT A REVISION PROCEDURE WHERE ALL SCREW SETS AND RODS OF RIGHT SIDE AT THE C5 AND C6 LEVELS WERE REMOVED ALONG WITH A LEFT SIDE ROD. NEW SCREWS WERE IMPLANT ON THE C5 LEVEL BUT NOT C6. NEW SCREW SET AND RODS WERE IMPLANTED ON BOTH SIDES AT THE C7 LEVELS.

    Patient problems: Numbness

    MAUDE report 8735071 ↗

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.