X-CORE 7180025Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517426291), received between Aug 7, 2017 and Aug 7, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Collapse” (1 report).

1 other recall cover devices cleared under the same FDA submission (K090176); they may or may not involve this specific model.

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

Recent adverse event reports

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

• MalfunctionAug 7, 2017Collapse; Device Slipped; Collapse; Device Slipped

  IN (B)(6) 2014, A PATIENT UNDERWENT A VERTEBRAL BODY REPLACEMENT PROCEDURE. IN A FOLLOW UP EXAM IT WAS DISCOVERED THAT THE IMPLANT HAD EXPERIENCED HEIGHT LOSS. THE PATIENT IS CURRENTLY ASYMPTOMATIC AND THERE ARE NO PLANS FOR REVISION SURGERY.

  Patient problems: Failure of Implant

  MAUDE report 6772800 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K090176. One submission often covers many models, so check the product and lot details in each record.

• Z-0738-2023 · Nov 10, 2022 · Open, Classified
  X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.