SONY LMD-2760MDRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04905524983111), received between Jul 7, 2020 and Dec 2, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 16, 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.

• MalfunctionDec 2, 2020No Display/Image; No Display/Image

  IT WAS REPORTED THAT DURING THE SET UP BEFORE THE SURGERY THE SONY 27 MONITOR IS POWERED ON, THE SCREEN HAS LINES ACROSS, AS PER THIS ISSUE, THE STAFF WAS UNABLE TO VIEW IMAGES. NO PATIENT INJURIES OR DELAY REPORTED. SMITH AND NEPHEW BACK-UP DEVICE WAS AVAILABLE TO COMPLETE THE SURGERY. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10932738 ↗
• MalfunctionJul 7, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT, AFTER THE PROCEDURE, A PARTIALLY RAW CABLE OF THE "SONY 27 MONITOR" CAUSED AN ELECTRICAL SHOCK TO A NURSE THAT TOUCHED THE SUPPORT OF THE MONITOR. IN CONSEQUENCE, SHE HAD TO BE SUPPORTED BY HOSPITAL FIRST AIDS. NO OTHER COMPLICATIONS WERE REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: Injury

  MAUDE report 10241014 ↗