Adult Anesthesia Circuit 9677Recalls & reported problems
Westmed, Inc. · 96" Adult Expandable Anesthesia Circuit · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00709078008290), received between Jun 3, 2022 and Jun 28, 2022 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (2 reports).
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.
Most reported problems
Device problems
- Material Split, Cut or Torn2
- Crack1
- Gas/Air Leak1
Patient problems
- Hypoxia1
- Insufficient Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 28, 2022Crack; Material Split, Cut or Torn
SPLITS/CRACKS IN TUBING THE CRNS EXTENDED THE TUBING AFTER INDUCTION AND AN OBVIOUS BREAK IN THE TUBING OCCURRED IN TWO PLACES. THIS WAS A SERIOUS SITUATION BECAUSE OF THE PATIENT'S COMORBIDITIES AND THE CONCERN FOR ETT IN ESOPHAGUS.
Patient problems: Insufficient Information
MAUDE report 14843216 ↗InjuryJun 3, 2022Gas/Air Leak; Material Split, Cut or Torn
SPLITS IN THE TUBING. THIS WAS DISCOVERED AFTER THE PATIENT BECAME HYPOXIC.
Patient problems: Hypoxia
MAUDE report 14597146 ↗
Other Filter, Bacterial, Breathing-Circuit devices
- VOCSN V+Pro, EnglishVentec Life Systems, Inc. · Filter, Bacterial, Breathing-Circuit1 recall570 reports
- VOCSN V+Pro Emergency, EnglishVentec Life Systems, Inc. · Filter, Bacterial, Breathing-Circuit558 reports
- VOCSN V+O+C+S+N+Pro, EnglishVentec Life Systems, Inc. · Filter, Bacterial, Breathing-Circuit3 recalls366 reports
- VOCSN V+Pro, EnglishVentec Life Systems, Inc. · Filter, Bacterial, Breathing-Circuit2 recalls2 deaths325 reports
- VOCSN V+C+S+N+Pro, EnglishVentec Life Systems, Inc. · Filter, Bacterial, Breathing-Circuit185 reports
- GIBECK IPN043751Teleflex Incorporated · Filter, bacterial, breathing-circuit2 recalls7 reports
- VOCSN VOCSN, EnglishVentec Life Systems, Inc. · Filter, Bacterial, Breathing-Circuit1 death96 reports
- VOCSN V+C+Pro, JapaneseVentec Life Systems, Inc. · Filter, Bacterial, Breathing-Circuit1 recall33 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page