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PowerFlexx® 0015800Recalls & reported problems

Ferno-Washington, Inc. · PowerFlexx® Powered Cot, Blue ST w/Univ Side Arm · Class 2

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 00190790000257), received between Apr 19, 2017 and Apr 19, 2017 — classified as 1 malfunction.

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

Most reported problems

Device problems

  • Mechanical Problem1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionApr 19, 2017Mechanical Problem; Mechanical Problem

    IT WAS REPORTED WHILE TRANSPORTING A PATIENT ON THE STRETCHER, THE X-FRAME BOLT ALLEGEDLY BROKE. NEITHER THE MEDIC CREW OR THE PATIENT WAS INJURED AND THE PATIENT WAS SAFELY TRANSFERRED TO ANOTHER STRETCHER TO CONTINUE THE TRANSPORT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 6502980 ↗

Other Stretcher, Wheeled devices

All Stretcher, Wheeled devices →

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