40" Carbon Fiber Extension 4-030-40Recalls & reported problems
Skytron LLC · 40" Carbon Fiber Extension for 3600B & 6700 SERIES · Class 1
Data updated Oct 18, 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 10841736112714), received between Apr 28, 2025 and Apr 28, 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 18, 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.
MalfunctionApr 28, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
A SKYTRON AUTHORIZED REPRESENTATIVE SUBMITTED A COMPLAINT DESCRIBING AN INCIDENT AT A CUSTOMER FACILITY WHERE A SKYTRON CARBON FIBER EXTENSION DETACHED FROM A SURGICAL TABLE WHILE THE SURGEON WAS TRYING TO RE-POSITION THE PATIENT. THERE WAS NO PATIENT INJURY REPORTED AS A RESULT OF THE INCIDENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21922447 ↗
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
- Medline PCD082021Medline Industries, Inc. · Surgical table cushion1 report
- NA Table PadSteris Corporation · 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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