Modulus 6793001P2Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517940933), received between Oct 18, 2024 and Oct 18, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Migration” (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

Recent adverse event reports

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

• MalfunctionOct 18, 2024Migration; Migration

  THE EVENT WAS IDENTIFIED DURING A REVIEW OF THE CERVICAL INTERBODY PMCF STUDY, THE REPORT IDENTIFIED THAT ON (B)(6) 2022 A PATIENT UNDERWENT A TWO LEVEL ANTERIOR CERVICAL DISCECTOMY FUSION PROCEDURE AT C4/5 AND C5/6. ON (B)(6) 2022 RADIOGRAPHIC IMAGING NOTED A SLIGHT SUBSIDENCE OF SUBJECTS C5/C6 INTERBODY. AT THE SAME FOLLOW UP, THE SUBJECT INDICATED DECREASED SENSATION OF THE FIRST 3 FINGERS OF THE RIGHT HAND. SUBJECT WILL CONTINUE FOLLOW UPS AND PI ORDERED AN EMG. NO REVISION IS PLANED AND THE PATIENT WILL CONTINUE TO BE MONITORED.

  Patient problems: Numbness

  MAUDE report 20485980 ↗