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PCM 7680259Recalls & reported problems

Nuvasive, Inc. · PCM V Disc, 5.9mm Small (US) · Class 3 · Implant

Data updated Oct 13, 2026 from official FDA records · Editorial policy

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 00887517601148), received between Jun 11, 2019 and Jun 11, 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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Numbness1
  • Pain1

Recent adverse event reports

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

  • InjuryJun 11, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    RECEIVED A VOLUNTARY REPORT THAT STATED, ON (B)(6) 2014, PATIENT UNDERWENT A CERVICAL PROCEDURE. POST-OPERATIVE PATIENT SUFFERED A CAR ACCIDENT. AS PER REPORTER NEUROSURGEON BELIEVES PCM IMPLANTED MAY BE TOO LARGE BASED ON MRI. AT THIS TIME PATIENT WILL NOT UNDERGO A REVISION PROCEDURE.

    Patient problems: Numbness; Pain

    MAUDE report 8689804 ↗

Other PROSTHESIS, INTERVERTEBRAL DISC devices

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Sources and updates

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