Disposable Anesthesia Circuit 9362Recalls & reported problems
Westmed, Inc. · Anesthesia Circuit, Adult, 120" Expandable Parallel WYE, GSE, Clear, 2L Latex Free Bag, B/V Filters, 10' x .050" GSL w Suction Tubing · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00709078006081), received between Sep 16, 2024 and Sep 19, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (3 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Loose or Intermittent Connection3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 19, 2024Loose or Intermittent Connection; Loose or Intermittent Connection
SUNMED HOLDINGS LLC. RECEIVED A SINGLE REPORT THAT REFERENCED THREE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING THREE DIFFERENT PATIENTS. THIS IS THE THIRD OF THREE REPORTS. REFER TO 2028807-2024-00032 FOR THE FIRST REPORT. REFER TO 2028807-2024-00045 FOR THE SECOND REPORT . IT WAS REPORTED, THE BLUE TUBING CONNECTOR FELL OFF, DURING PATIENT USE; THERE WAS NO REPORTED INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20260266 ↗MalfunctionSep 19, 2024Loose or Intermittent Connection; Loose or Intermittent Connection
SUNMED HOLDINGS LLC. RECEIVED A SINGLE REPORT THAT REFERENCED THREE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING THREE DIFFERENT PATIENTS. THIS IS THE SECOND OF THREE REPORTS. REFER TO 2028807-2024-00032 FOR THE FIRST REPORT, REFER TO 2028807-2024-00046 FOR THE THIRD REPORT. IT WAS REPORTED, THE BLUE TUBING CONNECTOR FELL OFF, DURING PATIENT USE; THERE WAS NO REPORTED INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20260099 ↗MalfunctionSep 16, 2024Loose or Intermittent Connection; Loose or Intermittent Connection
SUNMED HOLDINGS LLC. RECEIVED A SINGLE REPORT THAT REFERENCED THREE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING THREE DIFFERENT PATIENTS. THIS IS THE FIRST OF THREE REPORTS. REFER TO 2028807-2024-00045 FOR THE SECOND REPORT . REFER TO 2028807-2024-00046 FOR THE THIRD REPORT . IT WAS REPORTED, THE BLUE TUBING CONNECTOR FELL OFF, DURING PATIENT USE; THERE WAS NO REPORTED INJURY..
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20232773 ↗
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- 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.