UltraCare XT UCXTRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00857268006004), received between Oct 27, 2024 and Oct 27, 2024 — classified as 1 injury.

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

Recent adverse event reports

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

• InjuryOct 27, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED TO THE MANUFACTURER, BY THE END USER, PER THE END USER, THAT FAMILY CALLED IN A SERVICE TO HAVE LOWER RAILS ADDED TO HER DAD UCXT FRAME BECAUSE HE FELL OUT OF BED ON SATURDAY EVENING. HER SISTER WOKE UP IN THE MIDDLE OF THE NIGHT TO FIND THEIR DAD ON THE FLOOR NEXT TO THE BED. FAMILY CALLED THE PARAMEDICS TO PICK HIM UP AND PUT HIM BACK ON THE DOLPHIN SYSTEM. SHE HAD PLACED CHAIRS NEXT TO THE FRAME TO KEEP HIM FROM FALLING OUT AGAIN. SHE SAID HE DID NOT NEED ANY MEDICAL ATTENTION AND HE WAS NOT INJURED. I CREATED STAT SERVICE ORDER (B)(4) TO HAVE THE LOWER RAILS PLACED RIGHT AWAY. COMPLAINT #(B)(4) WAS ENTERED INTO OUR SYSTEM.

  Patient problems: Fall

  MAUDE report 20541448 ↗