SONY LMD-X310MDRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 04548736013940), received between Feb 5, 2018 and Apr 5, 2021 — classified as 4 malfunctions.

The most frequently reported specific device problem is “No Display/Image” (3 reports).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 5, 2021No Display/Image; No Display/Image

  IT WAS REPORTED THAT THE UHD 4K FLAT PANEL DISPLAY LCD (B)(6) 31" WAS FLICKERING AND HAD AN ORANGE SPOT IN THE MIDDLE OF THE SCREEN. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITHOUT DELAY. NO PATIENT INJURY OR 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: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11616898 ↗
• MalfunctionAug 8, 2020No Display/Image; No Display/Image

  IT WAS REPORTED THAT THE SONY MONITOR WAS NOT TURNING ON. THE DISPLAY WAS BLACK. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT. PRELIMINARY RESULTS OF INVESTIGATION HAVE CONCLUDED THAT HE THE DEVICE DOES NOT DISPLAY AN IMAGE WHICH MAKES IT A REPORTABLE EVENT. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

  Patient problems: No Patient Involvement

  MAUDE report 10383083 ↗
• MalfunctionJul 22, 2020No Display/Image; No Display/Image

  IT WAS REPORTED THAT THE PANEL DISPLAY POWER UP, THE LED LIGHTS ILLUMINATED A COUPLE OF MINUTES BUT THE DISPLAY HAD NO IMAGE. NO CASE REPORTED; THEREFORE, THERE WAS NO PATIENT INVOLVEMENT

  Patient problems: No Patient Involvement

  MAUDE report 10310956 ↗
• MalfunctionFeb 5, 2018Overheating of Device

  IT WAS REPORTED THAT THE MONITOR WAS UNUSUAL HEATED AFTER AN HOUR OF USE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7242322 ↗