EZ WIDER BARIATRIC BED ASM100130Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00850520008075), received between Jul 15, 2025 and Jul 15, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Device Handling Problem” (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.

• InjuryJul 15, 2025Device Handling Problem; Device Handling Problem

  ON (B)(6) 2025, PATIENT (B)(6) ATTEMPTED TO EGRESS THE EZ WIDER BED THROUGH THE HEAD / FOOT RAILS. HE DID NOT CALL FOR ASSISTANCE. THE PATIENT SLIPPED AND FELL HEADFIRST SUSTAINING ORAL INJURIES (NO OTHER HEAD TRAUMA REPORTED). THE PATIENT HAD SEIZURE PRECAUTIONS, ALSO NEEDING EEG DEVICES. FALL PADS WERE ALSO IN USE AT THE TIME. ONE FOOT RAIL WAS DOWN AT THE TIME. THE PATIENT WAS NOTED AS BEING 6' AND 101.8KG. (224LBS.). EDUCATOR BROOKE REACHED OUT TO KREG INQUIRING ABOUT NURSE CALL CABLES FOR OUR BEDS.THE BED DID NOT HAVE A NURSE CALL CABLE ATTACHED TO THE BED. THERE IS ALSO A QUESTION AS TO WHY THE BED WAS ORDERED FOR THE PATIENT, GIVEN THE PATIENT WAS 224 LBS.

  Patient problems: Fall

  MAUDE report 22512222 ↗