Uni-Lim Coaxial Circuit 9694Recalls & reported problems
Westmed, Inc. · 72" Adult Coaxial Circle Anesthesia Breathing CIrcuit · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00709078013652), received between Mar 14, 2025 and Jul 10, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Connection Problem” (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
- Connection Problem1
- Disconnection1
- Loose or Intermittent Connection1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 10, 2025Loose or Intermittent Connection; Connection Problem; Loose or Intermittent Connection; Connection Problem
WHILE ON PATIENT, THE CIRCUIT CAME OFF THE ANES MACHINES'S INSPIRATORY PORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22475238 ↗MalfunctionMar 14, 2025Disconnection; Disconnection
GAS SAMPLING ELBOW KEPT POPPING OFF FROM THE TUBING FROM MULTIPLE CIRCUITS BEFORE AND DURING THE CASES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21612808 ↗
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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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