Enterprise 9714DF101BCUSBRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05056097337272), received between Feb 20, 2026 and Feb 20, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

Recent adverse event reports

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

• MalfunctionFeb 20, 2026Detachment of Device or Device Component

  DURING THE PICK UP OF THE BED, IT WAS OBSERVED THAT THE LEFT HEAD SIDE RAIL WAS DAMAGED. THERE WAS NO INDICATION OF PATIENT INVOLVEMENT, AND NO INJURY WAS SUSTAINED. ADDITIONAL INFORMATION PROVIDED BY THE ARJO TECHNICIAN CONFIRMED THAT THE SIDE RAIL WAS DETACHED BECAUSE THE HOLDING-PANEL SCREWS HAD BEEN PULLED OUT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24398600 ↗