SONY LMD-X2705MDRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04548736100534), received between Apr 20, 2021 and Apr 20, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “No Display/Image” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 20, 2021No Display/Image; No Display/Image

  IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE, THE SONY 27 4K DISPLAY WHEN CONNECTED VIA THE DVI PORT, THE HE SCREEN WAS FLICKERING. THE PROCEDURE WAS COMPLETED WITH A DELAY OF 30 MINUTES OR LESS USING THE SAME DEVICE. 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 11694969 ↗