Modulus 67940068P2Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00887517984173), received between Feb 20, 2026 and Feb 20, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Unintended System Motion” (2 reports).

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 20, 2026Unintended System Motion

  THE SURGEON USED 2 SPINAL CAGES FOR ANTERIOR CERVICAL DISCECTOMY AND FUSION (ACDF). THE SURGEON REPORTED THAT THE CAGE HAD MOVED FORWARD 2 DAYS AFTER SURGERY, HE SHOULD PERFORM SURGERY AGAIN. THIS EVENT OCCURRED IN JAPAN. NO OTHER ADVERSE EFFECT REPORTED TO PATIENT.

  Patient problems: Failure of Implant; No Clinical Signs, Symptoms or Conditions

  MAUDE report 24405101 ↗
• MalfunctionFeb 20, 2026Unintended System Motion

  IT WAS REPORTED THAT THE SURGEON USED 2 SPINAL CAGES FOR ANTERIOR CERVICAL DISCECTOMY AND FUSION (ACDF). THE SURGEON INFORMED THAT THE CAGE MOVED FORWARD 2 DAYS AFTER SURGERY, HE SHOULD PERFORM SURGERY AGAIN. NO OTHER ADVERSE PATIENT CONSEQUENCES WERE REPORTED. THIS EVENT OCCURRED IN JAPAN AND IS REPORTABLE TO PMDA.

  Patient problems: Failure of Implant; No Clinical Signs, Symptoms or Conditions

  MAUDE report 24404575 ↗