NA PowerLift Plus (REF BF867)Recalls & reported problems
Steris Corporation · The PowerLift Plus Stirrups (pair) - Adult 500 with Pads is compatible with STERIS 3000, 4000, 5000 Series General Surgical Tables. · 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 00724995217280), received between May 29, 2025 and May 29, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Slipped” (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.
Reports received per month
Most reported problems
Device problems
- Device Slipped1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 29, 2025Device Slipped; Device Slipped
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR POWERLIFT PLUS STIRRUPS WOULD NOT REMAIN IN THE LOCK POSITION. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT REPORT OF DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22104404 ↗
Other STIRRUPS devices
- NA PowerLift PlusSteris Corporation · STIRRUPS1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.