NA Leg PositionerRecalls & reported problems
Steris Corporation · The Split Leg Positioner includes both Left and Right Leg Supports and provides a safe system for positioning patients for laparoscopic procedures and lower extremity Orthopedic and Vascular procedures. · 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 00724995225117), received between Jan 28, 2026 and Jan 28, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
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.
MalfunctionJan 28, 2026Break
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE A PIECE OF THE SPLIT LEG POSITIONER TO THEIR SURGICAL TABLE BROKE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY FOLLOWING A SHORT DELAY USING A DIFFERENT ACCESSORY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24200762 ↗
Other Table and attachments, operating-room devices
- Arthrex® AR-1747-BArthrex, Inc. · TABLE AND ATTACHMENTS, OPERATING-ROOM12 reports
- Arthrex® AR-1644Arthrex, Inc. · Table and attachments, operating-room5 reports
- Leg holder 100380A0MAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM4 reports
- Arthrex® AR-1560-02Arthrex, Inc. · TABLE AND ATTACHMENTS, OPERATING-ROOM4 reports
- Arthrex® AR-1500Arthrex, Inc. · TABLE AND ATTACHMENTS, OPERATING-ROOM3 reports
- Pair of leg plates 113373BCMAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM3 reports
- Kneeling frame 100704D0MAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM2 reports
- Traction boot, adult 10018800MAQUET GmbH · TABLE AND ATTACHMENTS, OPERATING-ROOM2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.