NuVasive 7175024Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517913333), received between Jan 27, 2022 and Jan 27, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Use of Device Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

• InjuryJan 27, 2022Use of Device Problem; Use of Device Problem

  ON (B)(6) 2022 A PATIENT UNDERWENT A POSTERIOR SPINAL PROCEDURE FROM L4-L5. DURING THE PROCEDURE A COMPETITOR BONE FUNNEL WAS INSERTED INTO THE DISC SPACE TO INSERT AUTOLOGOUS BONE WHEN BLEEDING WAS OBSERVED. HEMOSTASIS WAS PERFORMED, BUT BLOOD PRESSURE WAS LOW (50/30), SO THE PLANNED POSTERIOR FIXATION WAS NOT PERFORMED. THE PATIENT WAS TRANSPORTED TO OTHER FACILITY AND A STENT WAS PLACED. THE AMOUNT OF BLOOD LOSS IS UNKNOWN. THE BLEEDING WAS SUSPECTED TO HAVE OCCURRED ANTERIORLY AS THERE WAS A POSSIBILITY THE DISC WAS DAMAGED DURING CURETTAGE WITH THE RING CURETTE. THE ROOT CAUSE COULD NOT BE CONFIRMED. THE PATIENT IS RECOVERING WELL AND POSTERIOR FIXATION IS PLANNED TO BE PERFORMED AT A LATER DATE.

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 13367764 ↗