A&E Medical / Disposable Suction Coagulator 050-070Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10841291105039), received between Jul 1, 2019 and Jul 1, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Remains Activated” (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.

• MalfunctionJul 1, 2019Device Remains Activated; Device Remains Activated

  FDA MEDWATCH 3500A REPORT ((B)(4)) WAS RECEIVED ON 6/3/2019 ON BEHALF OF A USER-FACILITY INDICATING THE DEVICE FAILED TO DEACTIVATE ONCE THE ACTIVATOR WAS PRESSED AND HAD TO BE UNPLUGGED TO DEACTIVATE IT. USER-FACILITY INDICATED THE DEVICE HAD PATIENT CONTACT, HOWEVER, THERE WAS NO PATIENT HARM.

  Patient problems: Burn, Thermal; No Known Impact Or Consequence To Patient

  MAUDE report 8750812 ↗