NA PowerLift Plus (REF BF856)Recalls & reported problems

Steris Corporation · The PowerLift Plus Stirrups (pair) Kit - Adult 500 pounds with Pads and Secure-Release Clamps is compatible with STERIS 3000, 4000, 5000 Series General Surgical Tables. · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 00724995217198), received between Feb 26, 2025 and Feb 26, 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

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.

MalfunctionFeb 26, 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 21472531 ↗

Device details

UDI-DI	`00724995217198`
Brand	NA
Model	PowerLift Plus
Catalog no.	BF856
Company	Steris Corporation
Product code	EYD · STIRRUPS
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	—
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Dec 28, 2022

Device type (GMDN): Heel stirrup

A device used during a medical/surgical procedure to steadily hold a patient's foot (feet) by cradling the heel. It is typically attached to an operating table, examination table, or treatment chair and is considered an accessory to these devices. This device is typically constructed of metal and plastic and used in pairs mainly for patients in lithotomic position for obstetrical, urological, colonic, or rectal procedures. This is a reusable device.

Other STIRRUPS devices

NA PowerLift Plus
Steris Corporation · STIRRUPS
1 report

All STIRRUPS devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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