Anesthesia Circuit Kit 9810Recalls & reported problems
Westmed, Inc. · 72" Uni-lim™ coaxial circuit, patient elbow with capped gas sample port, M/M GSL 10' X .050ID X .108OD, 1 B/V filter, 3L latex-free breathing bag, disposable · Class 1
- 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 10889483609040), received between Mar 26, 2025 and Mar 26, 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. How this data works · Data updated Oct 13, 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.
MalfunctionMar 26, 2025Connection Problem; Connection Problem
SUNMED HOLDINGS LLC. RECEIVED A SINGLE REPORT THAT REFERENCED TWO DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWO DIFFERENT PATIENTS. THIS IS THE SECOND OF TWO REPORTS. REFER TO 2028807-2025-00012 FOR THE FIRST REPORT. IT WAS REPORTED, [WHILE] THE CIRCUIT WAS CONNECTED TO THE ANESTHESIA MACHINE THE FILTER HOUSING CAME LOOSE; [THE] CLINICIANS WERE UNABLE TO FIT IT BACK. THERE WAS NO REPORTED INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21700332 ↗
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- Anesthesia Circuit Kit Coax 3 MP02732Drägerwerk AG & Co. KGaA · Anesthesia Breathing Circuit Kit (Adult & Pediatric)1 recall0 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.