Endurance Deluxe Alternating Pressure Pump & Pad Combo D9000CRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00754756390013), received between Feb 16, 2017 and Feb 16, 2017 — classified as 1 death.

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.

• DeathFeb 16, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT'S SPOUSE FOUND HIM HANGING OVER THE SIDE OF BED, HEAD FIRST, AND WEDGED BETWEEN HOSPITAL BED AND WALL OF HOME. POLICE PRONOUNCED HIM DEAD AT SCENE. HOSPICE SERVICE FILED MEDWATCH REPORT ON ALL EQUIPMENT PRESENT AT THE SCENE. REVIEW OF SCENE PHOTOGRAPHS SHOW AN APP MATRESS SECURELY PLACED UNDER A CONTOUR SHEET; THE SHEET AND PAD REMAINED PROPERLY IN PLACE ON BED. THE APP SYSTEM APPEARS NON-CONTRIBUTORY IN PATIENT'S DEATH.

  Patient problems: Asphyxia; Death; Physical Entrapment

  MAUDE report 6336139 ↗