Aequalis Reversed II MWD150Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03700386972034), received between Dec 27, 2022 and Dec 27, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unintended System Motion” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 27, 2022Unintended System Motion; Unintended System Motion

  IT WAS REPORTED THAT THE REAMING OF THE JOINT FOSSA WAS NOT DONE PROPERLY DUE TO A LARGE SHAKE OF THE REAMER SHAFT. AND WHETHER DUE TO THIS OR SIMPLY A BAD BLADE ON THE 25MM BP REAMER, THE REAMING OF THE JOINT FOSSA WAS NOT DONE PROPERLY. THIS CAUSED DIFFICULTY IN SCREW ENTRY AND INSUFFICIENT THE BASE PLATE PLACEMENT (CONTACT AREA) ON THE JOINT SURFACE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16057875 ↗