Medline ASHA42500RHRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10888277669895), received between Dec 11, 2018 and Sep 24, 2026 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Component Missing” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 24, 2026Electrical /Electronic Property Problem; Overheating of Device

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50889988 ↗
• InjuryMar 10, 2023Material Integrity Problem; Material Integrity Problem

  ACCORDING TO THE CUSTOMER ON (B)(6) 2023 THE ABLATION WAND WAS FLAKING OFF INSIDE THE PATIENT DURING A SURGICAL PROCEDURE.

  Patient problems: Foreign Body In Patient

  MAUDE report 16525033 ↗
• MalfunctionDec 11, 2018Component Missing

  IT WAS REPORTED THAT DURING A SHOULDER ARTHROSCOPY, METAL MODES OF THE REPROCESSED AMBIENT¿ SUPER TURBOVAC¿ WERE NOTED TO BE MISSING REQUIRING IRRIGATION OF THE SURGICAL SITE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8150468 ↗