PAD SET WILSON FRAME TEMPUR PEDIC 5319-37Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842430102042), received between Mar 6, 2020 and Mar 6, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.

• MalfunctionMar 6, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THE PAD ON THE RIGHT SIDE SEEMS TO HAVE TO MUCH FLEXIBLE GIVE ON THE INSIDE. WHEN THEY LAY THE PATIENT DOWN ON TOP OF THE FRAME THE PAD SLIDES OUTWARDS CAUSING THE PLASTIC FRAME BENEATH THE PAD TO BE EXPOSED AND CAUSE PRESSURE RED MARKS ON THEIR PATIENTS.

  Patient problems: Erythema

  MAUDE report 9799225 ↗