Miranti CEB8003-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055982796293), received between Sep 6, 2022 and Sep 6, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Use of Device 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 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.

• MalfunctionSep 6, 2022Use of Device Problem; Use of Device Problem

  ARJO RECEIVED A CUSTOMER COMPLAINT WHERE IT WAS INDICATED THAT A RESIDENT WAS LYING ON THE MIRANTI BATH CHAIR WITH KNEES PULLED UP AND WITH SAFETY BAR ACROSS. THEN THE RESIDENT ROLLED OVER AND CAME OFF THE MIRANTI STRETCHER. THE CNA ATTEMPTED TO HOLD THE RESIDENT BUT THE RESIDENT SLID TO THE FLOOR. IT WAS REPORTED THAT THE RESIDENT WAS NOT SECURED BY SAFETY BELTS. AS A CONSEQUENCE OF THE FALL THE RESIDENT SUSTAINED A BRUISE ON THE TOP OF RIGHT HAND. NO MEDICAL INTERVENTION WAS REQUIRED.

  Patient problems: Fall

  MAUDE report 15360435 ↗