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Precept 8847150Recalls & reported problems

Nuvasive, Inc. · PRECEPT Ti Rod, 150mm Prebent Lordotic · 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 00887517378309), received between Jun 22, 2016 and Jun 22, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment Of Device Component” (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

  • Detachment Of Device Component1
  • Device Slipped1

Patient problems

  • No Information1

Recent adverse event reports

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

  • MalfunctionJun 22, 2016Detachment Of Device Component; Device Slipped; Detachment Of Device Component; Device Slipped

    ON (B)(6) 2016, A (B)(6) YEAR OLD MALE UNDERWENT 4-LEVEL INTERBODY FUSION L2-S1 WITH BILATERAL POSTERIOR PEDICLE SCREW INSTRUMENTATION. AROUND 3 MONTHS POSTOPERATIVE, IT WAS NOTED A ROD REPORTEDLY MIGRATED AND MULTIPLE LOCK SCREWS SEEM TO BE LOOSE.

    Patient problems: No Information

    MAUDE report 5743256 ↗

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