Disposable Anesthesia Circuits 9053Recalls & reported problems
Westmed, Inc. · 72" Exp. Pediatric Anesthesia circuit, par-wye, clear GSE, B/V Filter, GSL, 2L not made with latex breathing bag · 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 00709078011030), received between Sep 11, 2025 and Sep 11, 2025 — classified as 1 malfunction.
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Connection Problem1
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.
MalfunctionSep 11, 2025Connection Problem; Connection Problem
IT WAS REPORTED THAT THE CICUIT IS TO SHORT WHICH CAUSED A DISCONNECTION AND THE PROCEDURE WAS INTERRUPT WHEN CIRCUIT DISCONNECTED. THE CIRCUIT LENGTH DEPENDING ON HOW FAR THE ANESTHESIA MACHINE IS FROM THE ATTACHMENT. IF MOVED DURING PROCEDURE THERE MAY BE A POSSIBILITY FOR DISCONNECTION. ALTHOUGH, THERE WAS NO REPORT OF SERIOUS INJURY OR HARM TO PATIENT THERE WAS A DELAY IN THERAPY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23032573 ↗
Other Anesthesia Breathing Circuit Kit (Adult & Pediatric) devices
- AirLife™ 2K8000Airlife · Anesthesia breathing circuit kit (adult & pediatric)1 recall0 reports
- AirLife™ 2K8001Airlife · Anesthesia breathing circuit kit (adult & pediatric)1 recall0 reports
- Anesthesia Circuit Kit Coax 1 MP02730Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
- AirLife™ AH265Airlife · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
- AirLife™ AH265Airlife · Anesthesia breathing circuit kit (adult & pediatric)1 recall0 reports
- Anesthesia Circuit Kit Coax HEPA MP17102Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
- Anesthesia Circuit Kit Coax 3 MP02732Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
- Anesthesia Circuit Kit Flex 6 MP02744Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)6 reports
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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