Levó Dual Motion Base 7887-010Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00842430104657), received between Jul 23, 2018 and Mar 10, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device Slipped” (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 18, 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.

• MalfunctionMar 10, 2026Device Slipped

  IT WAS REPORTED THAT THE LEVO BASE WAS SLIPPING LATERALLY DURING 180 DEGREE ROTATIONS. AT FIRST IT WAS PERCEIVED THAT THE LATERAL LOCK WAS UNLOCKED BY AN ANESTHESIA LINE BUT LATER THE SLIP WAS NOTICED DUE TO THE MOMENTUM OF THE 180 DEGREE ROTATION.

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 24565097 ↗
• MalfunctionJul 23, 2018Unintended Movement; Unintended Movement

  DURING THE PROCEDURE WHEN DOCTOR WAS PLACING IN SCREWS INTO THE PATIENT SURGICAL AREA; THE LEVO LOCKS BECAME UNLOCKED AND THE LEVO DUAL MOTION BASE TILTED UP. THIS RESULTED INTO THE PATIENT HEAD TILTING DOWNWARD WHILE THE SURGEON WAS PLACING IN THE SCREWS.

  Patient problems: No Information; No Known Impact Or Consequence To Patient

  MAUDE report 7711653 ↗