Split Leg Section 4-030-61Recalls & reported problems
Skytron LLC · Split Leg Section for 6700 SERIES & 3600B · 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 10841736112745), received between May 20, 2025 and May 20, 2025 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
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 20, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
SKYTRON TECHNICAL SUPPORT RECEIVED A PHONE CALL FROM FROEDTERT MEMORIAL LUTHERAN HOSPITAL DESCRIBING AN INCIDENT INVOLVING A SKYTRON SPLIT LEG SECTION FOR 6700 SERIES & 3600B TABLE ACCESSORY. THE FACILITY ALLEGES THAT THEY WERE SET UP FOR A CASE AND WHEN THE TABLE WAS ADJUSTED TO REVERSE TRENDELENBURG POSITION THE SPLIT LEG ACCESSORY DISENGAGED FROM THE SURGICAL TABLE AND THE PATIENT SLID TO FOOT GOING INTO STRADDLE POSITION ON THE GROUND. NO PATIENT OR STAFF INJURIES WERE REPORTED AS A RESULT OF THE INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22056256 ↗
Other Surgical Table Cushion devices
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION6 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION5 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION4 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION3 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION2 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION2 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION1 report
- 40" Carbon Fiber Extension 4-030-40Skytron LLC · Surgical Table Cushion1 report
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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