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CONCERTO BAB1103-01Recalls & reported problems

Arjohuntleigh AB · CONCERTO SHOWER TROLLEY, 1900MM ELECTRIC, US · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05055982796163), received between Aug 11, 2023 and Aug 11, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Fell” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Device Fell1

Patient problems

  • Bruise/Contusion1
  • Fall1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 11, 2023Device Fell; Device Fell

    ARJO WAS NOTIFIED BY HEALTH CANADA OF AN INCIDENT RELATED TO THE CONCERTO SHOWER TROLLEY. IT WAS INDICATED THAT A PATIENT FELL FROM THE DEVICE AS THE LOCK FAILED. NO INJURIES WERE REPORTED. THE DEVICE WAS INSPECTED BY AN ARJO SERVICE TECHNICIAN. THE INSPECTION REVEALED THAT THE CONCERTO LOCKING MECHANISM CAN BE LOCKED AND UNLOCKED CORRECTLY. NO MALFUNCTION WAS FOUND. THERE WAS NOT POSSIBLE TO CONFIRM THE CUSTOMER ALLEGATION. THE ARJO SERVICE TECHNICIAN CLEANED AND LUBRICATED THE LOCKING MECHANISM AND PIVOT MECHANISM.

    Patient problems: Bruise/Contusion; Fall

    MAUDE report 17507770 ↗

Other Lift, Patient, Non-Ac-Powered devices

All Lift, Patient, Non-Ac-Powered devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.