Century AK61611-USRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055982701068), received between Oct 20, 2022 and Oct 20, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unintended System Motion” (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.

• MalfunctionOct 20, 2022Unintended System Motion; No Apparent Adverse Event; Unintended System Motion; No Apparent Adverse Event

  ARJO BECAME AWARE OF AN EVENT WITH A CENTURY BATH. IT WAS INDICATED THAT THE BATH CAME OFF ("BUMPED OUT OF") THE BRACKET DURING USE WITH A RESIDENT. THERE WERE NO REPORTED INJURIES TO THE RESIDENT AND UNKNOWN MINOR INJURIES TO THE CAREGIVER. DESPITE MANY ATTEMPTS, THE CIRCUMSTANCES UNDER WHICH THE FAILURE OCCURRED WERE NOT DISCLOSED BY THE CUSTOMER. BASED ON INFORMATION RECEIVED FROM AN ARJO TECHNICIAN WHO ATTEMPTED TO OBTAIN MORE DETAILS, IT IS KNOWN THAT THE FLOOR IN THE CUSTOMER'S FACILITY IS UNEVEN. HE INFORMED THAT THE FACILITY STAFF INDICATED THAT THE RESIDENT WAS ON THE ALENTI BATH CHAIR AND THE CAREGIVER WAS ASSISTING THE RESIDENT TO GET OUT OF THE BATH CHAIR. AT THIS MOMENT THE BACK WHEEL OF THE ALENTI MOVED CAUSING THE RESIDENT TO FALL ONTO THE CAREGIVER. HOWEVER, THE ALENTI INCIDENT IS NOT THE SUBJECT OF THIS REPORT AND WAS EVALUATED UNDER REPORT 3007420694-2022-00169. THIS REPORT IS RELATED TO CENTURY BATH ISSUE REPORTED.

  Patient problems: Fall

  MAUDE report 15637937 ↗